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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976630Generated: October 25, 2026

Ammonium formate → tert-butyl N-hydroxy-N-(2-methylpropyl)carbamate

https://huagongshe.com/reaction/976630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactanttert-butyl N-benzyloxy-N-(2-methylpropyl)carbamateHCID 19967428—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-butyl N-hydroxy-N-(2-methylpropyl)carbamateHCID 1996744299.1%

Reaction Steps

Ammonium formate (7.9 g, 125 mmol) and 10% palladium on carbon (2 g) were added to a solution of tert-butyl-N-benzyloxy-N-(2-methylpropyl)carbamate (Compound 54 Part B, 6.27 g, 22.4 mmol) in ethanol (100 mL). The reaction mixture was stirred at ambient temperature for 5 hours then concentrated under vacuum at 50° C. The residue was taken up in methylene chloride, washed with water, dried with magnesium sulfate and then concentrated to provide 4.2 g of tert-butyl N-hydroxy-N-(2-methylpropyl)carbamate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05612377
Source datasetuspto-grants-1997_03
ORD IDord-f0ababa71772444b91273ae6bc67f214
Source noteuspto-grants-1997_03