药物合成反应(闻韧_第三版)第二章课后答案Chapter_2_Alkylation_Reaction

1、药物合成反应 （第三版）闻韧主编习题及答案第二章 烃化反应习题及答案1. 根据以下指定原料、试剂和反应条件，写出其合成反应的主要产物(1)oho+h3po4 / bf3oet2(2)brbrch3liether(3)no2ch2brco2ch3och3rnh2et3n/meoh(4)knoohnoophoms+dmfh2nnh2h2oetoh, 60oc(5)inh2o+dabco, dmf(6)meoomeome2nh, meohr.t.(7)meonhso2no2ph(ch2)3brk2co3, dmf(8) phch2ch2mgbr +nchothf1武汉工程大学化工与制药学院药物合成反

2、应 （第三版）闻韧主编习题及答案(9)broachme1) c5h11o k2) c5h11oh(10)oobrome+sncl40oc1. 根据以下指定原料、试剂和反应条件，写出其合成反应的主要产物（参考答案）题号答案注释(1) ooc(ch3)3(2) ch3ch3(3) no2och3nromu f., et al. j. med. chem., 2002, 45: 4774. (4) hnoophnoohnoophnh2rossi f. m., et al. tetrahedron, 1996, 52: 10279. (5) nhdabco= 1,4-diazabicyclo2.2.2

3、octane nn2药物合成反应 （第三版）闻韧主编习题及答案(6) me2no(7) meonso2no2(8) phch2ch2cho (9) ohh3c(10) oomeo待核对原始文献！patil m. l., et al. tetra. lett., 1999, 40: 4437. 2. 在下列指定原料和产物的反应式中分别填入必需的化学试剂（或反应物）和反应条件。(1)ch2co2me(2)oohooohor(3) ch2(co2et)2co2hco2h(4)oohoh2cch2ohoophh2coh2cch2och2ph3药物合成反应 （第三版）闻韧主编习题及答案(5)ohno2o

4、ch2phno2(6)otfcl+nhphmenclmeph(7)oso2phoph(8)nchoohnchooch3(9)etoetoo(10)meomebrmeomehnhex2. 在下列指定原料和产物的反应式中分别填入必需的化学试剂（或反应物）和反应条件。（参考答案）题号答案注释(1) 1. na; 2. brch2co2me (2) 1. 2 lda, 2. rx (3) 1,2-dibromoethane, teba, oh(4) nah, phch2br, thf (5) phch2cl, k2co3, dmf (6) cat. pd(oac)2, ()-binap, cs2co3

5、, thf, 70(7) phcch, i-prmgcl, znbr2, thf (8) mei, nah, thf (9) 1. lda, thf, -78; 2. mei, -78 to 25 (10) hexnh2, pd2(dba)3 ()-binap, t-buona, toluene hex= hexyl dba= dibenzylideneacetone 4药物合成反应 （第三版）闻韧主编习题及答案o3. 阅读（翻译）以下有关反应操作的原文，请在理解基础上写出：（1）此反应的完整反应式（原料、试剂和主要反应条件） ； （2）此反应的反应机理（历程）。（1）preparation

6、of cyclopropane 1,l-dicarboxylic acid to a 1-l solution of aqueous 50% sodium hydroxide (note 1), mechanically stirred in a 2-l, three-necked flask, was added, at 25c, 114.0 g (0.5 mol) of triethylbenzylammonium chloride (note 2). to this vigorously stirred suspension was added a mixture of 80.0 g (

7、0.5 mol) of diethyl malonate and 141.0 g (0.75 mol) of 1,2-dibromoethane all at once. the reaction mixture was vigorously stirred for 2 hr (note 3). the contents of the flask were transferred to a 4-l erlenmeyer flask by rinsing the flask with three 75-ml portions of water. the mixture was magnetica

8、lly stirred and cooled with an ice bath to 15c, and then carefully acidified by dropwise addition of 1 l of concentrated hydrochloric acid. the temperature of the flask was maintained between 15 and 25c during acidification. the aqueous layer was poured into a 4-l separatory funnel and extracted thr

9、ee times with 900 ml of ether. the aqueous layer was saturated with sodium chloride and extracted three times with 500 ml of ether. the ether layers were combined, washed with 1 l of brine, dried (mgso4), and decolorized with activated carbon. removal of the solvent by rotary evaporation gave 55.2 g

10、 of a semisolid residue. the residue was triturated with 100 ml of benzene. filtration of this mixture gave 43.147.9 g (6673%) of 1 as white crystals, mp 137140c. （2）preparation of mesitaldehyde (2,4,6-trimethyl benzaldehyde) a solution of 72 g. (0.60 mole) of mesitylene in 375 ml. of dry methylene

11、chloride is placed in a 1-l. three-necked flask equipped with a reflux condenser, a stirrer, and a dropping funnel. the solution is cooled in an ice bath, and 190 g. (110 ml., 1.0 mole) of titanium tetrachloride is added over a period of 3 minutes. while the solution is stirred and cooled, 57.5 g. (

12、0.5 mole) of dichloromethyl methyl ether2 is added dropwise over a 25-minute period. the reaction begins (as indicated by evolution of hydrogen chloride) when the first drop of chloro ether is added. after the addition is complete, the mixture is stirred for 5 minutes in the ice bath, for 30 minutes

13、 without cooling, and for 15 minutes at 35. the reaction mixture is poured into a separatory funnel containing about 0.5 kg. of crushed ice and is shaken thoroughly. the organic layer is separated, and the aqueous solution is extracted with two 50- ml. portions of methylene chloride. the combined or

14、ganic solution is washed three times with 75-ml. portions of water. a crystal of hydroquinone is added to the methylene chloride solution (note 1) which is then dried over anhydrous sodium sulfate. after evaporation of the solvent, the residue is distilled to give the crude product, b.p. 6874 (0.9 mm.). after redistillation there is obtained 6066 g. (8189%) of mesitaldehyde; b.p. 113115 (11 mm.)