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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028201Generated: October 25, 2026

Methanol → HCID 178500705, compound

https://huagongshe.com/reaction/1028201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 2-(4-oxocyclohexyl)acetateHCID 21249113—
SolventAmmonium ChlorideHCID 25517—
ProductMethyl AcetateHCID 658412%
ProductHCID 178500705HCID 17850070560%

Reaction Steps

To a methanol (50 mL) solution of (4-oxo-cyclohexyl)-acetic acid methyl ester (4.18 g) obtained in Example (1c), sodium borohydride (1.86 g) was added in small portions at 0° C. The reaction mixture was stirred for 1 hour and diluted with a 10% aqueous ammonium chloride solution (100 mL). The organic solvent was removed using an evaporator. The remaining aqueous solution was subjected to two extractions with ethyl acetate. The organic layer was washed with saturated brine, then dried over sodium sulfate, and then concentrated to obtain trans-(4-hydroxy-cyclohexyl)-acetic acid methyl ester (2.56 g, 60%) as a colorless oil and cis-4-hydroxy-cyclohexyl)-acetic acid methyl ester (0.517 g, 12%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735425B2
Source datasetuspto-grants-2014_05
ORD IDord-d4684c1b85a14155b25f0b7dc763c42e
Source noteuspto-grants-2014_05