반응 #2650

ord-722e940fd7a54e458d6fcaedb1602d00

반응 방정식

O.[Li+].[OH-]
lithium hydroxide monohydrate
ClC(Cl)Cl
chloroform
CC(=O)O[C@@H]1C=C[C@H](OC(C)(C)C)C1
(-)-acetic acid cis-4-tert-butyloxy-cyclopent-2-enyl ester
O
water
CC(C)(C)O[C@H]1C=C[C@@H](O)C1
title compound
수율 101.0%
CC(C)(C)O[C@H]1C=C[C@@H](O)C1
(+)-cis-4-tert-butyloxy-cyclopent-2-enol
수율 101.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONdilute
  2. 2
    추출extract with tert-butyl methyl ether
  3. 3
    건조dry over anhydrous magnesium sulfate
  4. 4
    여과filter
  5. 5
    농축concentrate under vacuum
  6. 6
    기타Purify 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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05728899uspto-grants-1998_03