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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961632Generated: October 31, 2026

Ammonium Chloride → rel-1,1-Dimethylethyl N-[[(1R,2R)-2-(hydroxymethyl)cyclobutyl]methyl]carbamate

https://huagongshe.com/reaction/1961632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 66627373HCID 66627373—
SolventMethanolHCID 887—
Productrel-1,1-Dimethylethyl N-[[(1R,2R)-2-(hydroxymethyl)cyclobutyl]methyl]carbamateHCID 66625985100%

Reaction Steps

To a solution of Trans-2-(tert-Butoxycarbonylamino-methyl)-cyclobutanecarboxylic acid methyl ester (4.1 g, 16.8 mmol) in methanol (20 mL) at 0° C., sodium Borohydride (1.3 g, 33.6 mmol) was added portionwise. The mixture was stirred 4 h until TLC after TLC indicated completion of the reaction. A saturated solution of ammonium chloride was added, the methanol was removed under vacuum and the water was extracted three times with dichloromethane. The combined organic layers were washed with water and brine, dried over magnesium sulfate, filtered, evaporated and purified with column chromatography on silica gel using n-Heptane-EtOAc (1:1). The product fractions were concentrated to give 2.8 g (16.8 mmol, 80% yield) of the title compound as a white solid. MS (m/e): 216.3 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415350B2
Source datasetuspto-grants-2013_04
ORD IDord-6ba6d950d74d494c95070c65fc29039b
Source noteuspto-grants-2013_04