Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408955Generated: November 2, 2026

Diethyl Ether → (+/-)-benzyl (1S,2S)-2-hydroxy-2-methylcyclohexylcarbamate

https://huagongshe.com/reaction/1408955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantBenzyl (2-oxocyclohexyl)carbamateHCID 14219048—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
Product(+/-)-benzyl (1S,2S)-2-hydroxy-2-methylcyclohexylcarbamateHCID 8670770688%

Reaction Steps

Benzyl 2-oxocyclohexylcarbamate (173 mg, 0.7 mmol) in THF (3 mL) was cooled to −78° C. and added MeMgBr in ether (0.7 mL, 2.1 mmol) dropwise via syringe. The ice bath was removed and the reaction was allowed to stir at rt for 3 h. The reaction was quenched with sat. aqueous NH4Cl (1 mL) and partitioned between ethyl acetate and water. The layers were separated and the organic layer washed with brine, dried (Na2SO4), filtered and concentrated. The product was subjected to flash chromatography on silica gel (10% to 70% ethyl acetate/hexanes) to afford the title compound (81 mg, 88% yield) as a single diastereomer. This material was used as is in the next transformation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921368B2
Source datasetuspto-grants-2014_12
ORD IDord-2765bb223ed54ee18e0c1cfffa1e0a65
Source noteuspto-grants-2014_12