Hydrochloric Acid → Diethyl benzylsuccinate
반응식
[C:1]1([CH2:7][C:8](C(OCC)=O)([C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl>>[C:1]1([CH2:7][CH:8]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1참가 물질
3
실험 절차
A solution of the product from step (a) (23.6 g) in c.HCl (326 ml) was stirred under reflux for 46 hours, then cooled. The resulting precipitate was extracted with chloroform (×3) and the extracts combined, washed with 2M aqu. KOH (×2), acidified to pH 4.0 (2M aqu. HCl) and cooled. The resulting precipitate was filtered off, washed with water and dried in vacuo to give the desired product (15.7 g). The 200 MHz 1H NMR was consistent with the proposed structure.
후처리
- temperatureunder reflux for 46 hours
- temperaturecooled
- extractionThe resulting precipitate was extracted with chloroform (×3)
- washwashed with 2M aqu
- temperaturecooled
- filtrationThe resulting precipitate was filtered off
- washwashed with water
- customdried in vacuo
출처 및 근거
- ORD 기록
- ord-bc07f67c065949cfb8820a459ba7ce85
- 출처 데이터셋
- uspto-grants-1993_07
- 특허 번호
- US05225431
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