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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966071Generated: October 30, 2026

Water → ((1r,4r)-4-((Benzyloxy)methyl)cyclohexyl)methanol

https://huagongshe.com/reaction/1966071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178520956HCID 178520956—
CatalystTetrabutylammonium IodideHCID 67553—
SolventTetrahydrofuranHCID 8028—
Product((1r,4r)-4-((Benzyloxy)methyl)cyclohexyl)methanolHCID 2210676360%

Reaction Steps

To a slurry of NaH (440 mg, 11 mmol) in THF (22 mL) is added trans-1,4-cyclohexanedimethanol (1.44 g, 10 mmol) at 0° C., and the mixture is stirred for 1 hour while warming to room temperature. Benzyl bromide (1.2 mL, 10 mmol) is added dropwise followed by TBAI (185 mg, 0.5 mmol). The reaction is heated to 60° C. for 15 hours. After cooling to room temperature, H2O is added, and the mixture is extracted with EtOAc. The combined organic layer after dried over MgSO4 is concentrated to obtain (4-benzyloxymethyl-cyclohexyl)-methanol as clear oil (1.40 g, 60%) after purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420641B2
Source datasetuspto-grants-2013_04
ORD IDord-c6b054a247b44ff79a6016210ed95a42
Source noteuspto-grants-2013_04