반응식
O=O.[C:3]([OH:11])(=[O:10])[C:4]([CH2:6][C:7]([OH:9])=[O:8])=[CH2:5].C1(C)C=CC=CC=1.C(N(CC)CC)C>CC(OC(N1[C@H](CP(C2C=CC=CC=2)C2C=CC=CC=2)C[C@H](P(C2C=CC=CC=2)C2C=CC=CC=2)C1)=O)(C)C.FC(F)(F)C([O-])=O.C([N+](CCCC)(CCCC)CCCC)CCC.CO>[CH3:5][CH:4]([CH2:6][C:7]([OH:9])=[O:8])[C:3]([OH:11])=[O:10]참가 물질
실험 절차
A 500 ml steel autoclave was loaded in a glove box (O2 -content less than 1 ppm) with 2.6 g (20 mmol) of itaconic acid, 150 ml of toluene, 50 ml of methanol, 2.02 g (20 mmol) of triethylamine, 36.0 mg (0.0886 mmol) of [Rh(COD)2 ]BF4, 49 mg (0.0886 mmol) of BPPM and 31.5 mg (0.0886 mmol) of tetrabutylammonium trifluoroacetate. the hydrogenation was carried out at a constant pressure of 6 bar of H2, at 30° C. and with intensive stirring. After a total hydrogenation time of 3 hours the reaction solution was evaporated and the residue was dissolved in 40 ml of 2N sodium hydroxide solution. The aqueous phase was washed with toluene, adjusted to pH 2 with conc. hydrochloric acid, saturated with NaCl and extracted with 3×100 ml of ether. The combined ether phases were dried over Na2SO4 and evaporated. There were obtained 2.4 g (92.3%) of methylsuccinic acid as white crystals. M.p. 111°-112° C. [α]D20 =-16.2° (c=5, EtOH). Optical purity 95.4%.
후처리
- customwas carried out at a constant pressure of 6 bar of H2, at 30° C. and with intensive stirring
- customAfter a total hydrogenation time of 3 hours the reaction solution was evaporated
- dissolutionthe residue was dissolved in 40 ml of 2N sodium hydroxide solution
- washThe aqueous phase was washed with toluene
- extractionextracted with 3×100 ml of ether
- dry with materialThe combined ether phases were dried over Na2SO4
- customevaporated
출처 및 근거
- ORD 기록
- ord-10583bfae725468e9475ee4ead696f81
- 출처 데이터셋
- uspto-grants-1987_03
- 특허 번호
- US04652657
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