반응 #2650
ord-722e940fd7a54e458d6fcaedb1602d00
반응 방정식
lithium hydroxide monohydrate
chloroform
(-)-acetic acid cis-4-tert-butyloxy-cyclopent-2-enyl ester
water
→
title compound
수율 101.0%
(+)-cis-4-tert-butyloxy-cyclopent-2-enol
수율 101.0%
반응물
시약
없음
반응 조건
상세 조건
See reaction.notes.procedure_details.
후처리
- 1workup.ADDITIONdilute
- 2추출extract with tert-butyl methyl ether
- 3건조dry over anhydrous magnesium sulfate
- 4여과filter
- 5농축concentrate under vacuum
- 6기타Purify the residue by flash chromatography (silica gel, 2 g, 40% diethyl ether/hexane, 1.5×2.5 cm column)
실험 절차
Dissolve (-)-acetic acid cis-4-tert-butyloxy-cyclopent-2-enyl ester (90 mg, 0.45 mmol, prepared in example 14) in THF/methanol/water (1.5/0.5/0.5 mL). Add lithium hydroxide monohydrate (23.7 mg) with stirring. After stirring for about 2 hours at room temperature, dilute the reaction with water (10 mL) and extract with tert-butyl methyl ether. Combine the organic phases, dry over anhydrous magnesium sulfate, filter and concentrate under vacuum. Purify the residue by flash chromatography (silica gel, 2 g, 40% diethyl ether/hexane, 1.5×2.5 cm column) to provide the title compound (71 mg, quantitative yield, 76% ee) as a pale yellow oil, [α]20 D =+14.6°, (c=1.03, chloroform).