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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 66627373 | HCID 66627373 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | rel-1,1-Dimethylethyl N-[[(1R,2R)-2-(hydroxymethyl)cyclobutyl]methyl]carbamate | HCID 66625985 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415350B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-6ba6d950d74d494c95070c65fc29039b |
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| Source note | uspto-grants-2013_04 |
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