Hydrochloric Acid → [6-(Hydroxymethyl)-3-cyclohexenyl]-N-octadecylformamide
반응식
[CH2:1]([N:19]1[C:27](=O)[CH:26]2C(C[CH:23]=[CH:24][CH2:25]2)[C:20]1=[O:29])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].C[CH:31]([OH:33])[CH3:32].[BH4-].[Na+].Cl>O>[OH:33][CH2:31][CH:32]1[CH:27]([N:19]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[CH:20]=[O:29])[CH2:26][CH:25]=[CH:24][CH2:23]1참가 물질
6
실험 절차
2-Octadecyl-4,7,3a,7a-tetrahydroisoindole-1,3-dione (5.00 g) was suspended into a mixture of 2-propanol (90 ml) and water (15 ml) and then sodium borohydride (2.34 g) was added thereto. After being stirred for 46 hours at room temperature, the reaction mixture was acidified with dilute hydrochloric acid and then concentrated. The residue was, with chloroform added thereto, washed with dilute hydrochloric acid, water and saturated sodium hydrogencarbonate aqueous solution successively, dried over sodium sulfate anhydride, and concentrated. The residue was purified by silica gel column chromatography (silica gel 80 g, chloroform:methanol=50:1-10:1), thereby yielding the entitled compound (4.32 g) as white crystals.
후처리
- concentrationconcentrated
- additionadded
- washwashed with dilute hydrochloric acid, water and saturated sodium hydrogencarbonate aqueous solution successively
- dry with materialdried over sodium sulfate anhydride
- concentrationconcentrated
- customThe residue was purified by silica gel column chromatography (silica gel 80 g, chloroform:methanol=50:1-10:1)
출처 및 근거
- ORD 기록
- ord-a05458d6b26d497282ef231344e0aa16
- 출처 데이터셋
- uspto-grants-2001_01
- 특허 번호
- US06174885B1
반응 노트
불러오는 중…