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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394155Generated: November 1, 2026

Lithium Hydroxide → 5(S)-(Boc-Amino)-4(S)-hydroxy-6-cyclohexyl-2(R)-[(2,3,4-trimethoxyphenyl)methyl]hexanoic acid

https://huagongshe.com/reaction/2394155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
Reactant5(S)-[1(S)-(Boc-Amino)-2-cyclohexylethyl]-3(R)-[(2,3,4-trimethoxyphenyl)-methyl]dihydrofuran-2-(3H)-oneHCID 67709387—
SolventCitric AcidHCID 311—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventAmmonium ChlorideHCID 25517—
Product5(S)-(Boc-Amino)-4(S)-hydroxy-6-cyclohexyl-2(R)-[(2,3,4-trimethoxyphenyl)methyl]hexanoic acidHCID 22876397—

Reaction Steps

A solution of 600 mg (1.22 mmol) of 5(S)-[1(S)-(Boc-amino)-2-cyclohexylethyl]-3(R)-[(2,3,4-trimethoxyphenyl)methyl]dihydrofuran-2-(3H)-one in 20 ml of dimethoxyethane and 9.9 ml of water is treated, at RT, with 4.9 ml of a 1M solution of lithium hydroxide in water, and this reaction mixture is stirred for 2 h. It is then transferred to a separating funnel and diluted with 60 ml of sat. ammonium chloride solution and 5 ml of a 10% citric acid solution (both being cold); this mixture is then extracted with ethyl acetate and a little THF. The title compound, which is dried under HV and subjected to further processing without being purified, is obtained after washing the organic phase with (cold) saline and drying it over sodium sulfate. IR(CH2 Cl2) inter alia: 3431, 1710, 1602, 1495, 1165 and 1100 cm-1. FAB-MS (M+H)+ =510. HPLC tRet =16.13 min (gradient II).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05807891
Source datasetuspto-grants-1998_09
ORD IDord-59c1e2ee95274749b5366c3756bd5b90
Source noteuspto-grants-1998_09