Sodium Hydroxide → 3,4-Dihydro-6-(phenylmethoxy)-2-naphthalenecarboxylic acid
반응식
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][CH:18]=1)[CH:15](O)[CH:14]([C:20]([OH:22])=[O:21])[CH2:13][CH2:12]2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+]>CO>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]2[C:16]([CH:15]=[C:14]([C:20]([OH:22])=[O:21])[CH2:13][CH2:12]2)=[CH:17][CH:18]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1참가 물질
실험 절차
Methyl ester of 6-benzyloxy-1-hydroxy-1,2,3,4-tetrahydro-2-naphthoic acid (0.6 g) is dissolved in methanol (50 ml). To the solution is added an aqueous solution (10 ml) of sodium hydroxide (2 g), and the mixture is left standing for 30 minutes at room temperature. The resultant is concentrated under reduced pressure. The concentrate is diluted with water (50 ml). The precipitating crystals are collected by filtration. This product is dissolved in a mixture of dioxane (50 ml) and concentrated hydrochloric acid (2 ml). The mixture is left standing for 5 minutes at 80° C. and then for 30 minutes at room temperature. The resultant is concentrated under reduced pressure. Water (50 ml) is added to the concentrate. The precipitating crystals are collected by filtration to give 7-benzyloxy-1,2-dihydro-3-naphthoic acid (0.45 g) as colorless crystals, followed by recrystallization from a mixture of methanol and acetone to afford colorless needles, m.p. 202°-205° C.
후처리
- waitthe mixture is left
- concentrationThe resultant is concentrated under reduced pressure
- additionThe concentrate is diluted with water (50 ml)
- filtrationThe precipitating crystals are collected by filtration
- dissolutionThis product is dissolved in a mixture of dioxane (50 ml) and concentrated hydrochloric acid (2 ml)
- waitThe mixture is left
- waitstanding for 5 minutes at 80° C.
- waitfor 30 minutes at room temperature
- concentrationThe resultant is concentrated under reduced pressure
- additionWater (50 ml) is added to the concentrate
- filtrationThe precipitating crystals are collected by filtration
출처 및 근거
- ORD 기록
- ord-c2d425b448184586907ebbbe175e633e
- 출처 데이터셋
- uspto-grants-1989_11
- 특허 번호
- US04880809
반응 노트
불러오는 중…