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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269350Generated: October 31, 2026

Methanol → (2R,3R)-3-hydroxy-2-(4-phenylcyclohexylmethyl)butanoic acid

https://huagongshe.com/reaction/2269350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantMethyl (2R,3R)-3-Hydroxy-2-(4-phenylcyclohexylmethyl)butanoateHCID 57272933—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(2R,3R)-3-hydroxy-2-(4-phenylcyclohexylmethyl)butanoic acidHCID 5730116489%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of methyl (2R,3R)-3-hydroxy-2-(4-phenylcyclohexylmethyl)butanoate (4.17 g, 0.014 mol) and lithium hydroxide monohydrate (0.59 g, 0.014 mol) is stirred at 25° C. in a mixture of THF (30 mL), methanol (15 mL) and water (15 mL) for 72 h. The reaction is not complete and an additional 0.88 g (0.021 mol) of lithium hydroxide monohydrate in water (10 mL) is added. After 6 h an additional 0.59 g (0.014 mol) of solid lithium hydroxide monohydrate and the mixture is stirred at 25° C. for 18 h. The mixture is concentrated in vacuo and the residue is taken up in water, chilled in an ice-bath and the pH is adjusted to 2 with sodium bisulfate. The mixture is extracted with dichloromethane. The combined extracts were washed with saturated sodium chloride, dried over sodium sulfate and concentrated in vacuo to give 3.43 g (89%) of (2R,3R)-3-hydroxy-2-(4-phenylcyclohexylmethyl)butanoic acid as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329400B1
Source datasetuspto-grants-2001_12
ORD IDord-a3968a2575be41d6a32bf969b4a23bf1
Source noteuspto-grants-2001_12