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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340776Generated: October 26, 2026

Water → Methyl 3-hydroxycyclohexane-1-carboxylate

https://huagongshe.com/reaction/340776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantMethyl 3-oxocyclohexane-1-carboxylateHCID 566099—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductMethyl 3-hydroxycyclohexane-1-carboxylateHCID 12209242—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-oxo-1-cyclohexanecarboxylic acid methyl ester (1.1 g, 7.04 mmol) was dissolved in methanol (25 ml) and cooled to 0° C. under N2. Sodium borohydride (0.550 g, 14.54 mmol) was added in portions and the resulting solution stirred at 0° C. for 2 h. The solution was then diluted by the dropwise addition of water, followed by EtOAc (100 mL). The aqueous phase was separated and extracted with EtOAc (2×50 ml). The combined organic layers were washed with brine, dried over sodium sulphate, and concentrated in vacuo to give the title compound. TLC: 40% EtOAc/hexanes, high Rf: 0.4, low Rf: 0.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895596B2
Source datasetuspto-grants-2014_11
ORD IDord-51efb87b148a4233b5eb57f52374eadc
Source noteuspto-grants-2014_11