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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171597Generated: October 31, 2026

HCID 86596909, compound → HCID 86610537, compound

https://huagongshe.com/reaction/1171597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86596909HCID 86596909—
SolventAcetic AcidHCID 176—
SolventAcetonitrileHCID 6342—
ProductHCID 86610537HCID 8661053783%

Reaction Conditions

Temperature60 °C

Reaction Steps

A sample of benzyl (1S,2R,4R)-4-methoxy-2-(trityloxymethyl)cyclohexylcarbamate (0.53 g) was dissolved in a mixture of 70% aqueous acetic acid (10 mL) and MeCN (10 mL) and stirred at 60° C. for 2 h. Reaction mixture was cooled and evaporated. Dissolved in EtOAc and washed with saturated NaHCO3 followed by brine and then dried (MgSO4). Filtered, concentrated and chromatographed to get benzyl (1S,2R,4R)-2-(hydroxylmethyl)-4-methoxycyclohexylcarbamate (0.24 g, yield=83%) as a clear oil. MS found: (M+H)+=294.29.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829571B2
Source datasetuspto-grants-2010_11
ORD IDord-f63c010ebe6042ad9f5aaf5d56aa5a46
Source noteuspto-grants-2010_11