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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874364Generated: November 1, 2026

Sodium Methoxide → Tert-butyl (2-fluoro-5-hydroxyphenyl)carbamate

https://huagongshe.com/reaction/1874364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 57749294HCID 57749294—
SolventMethanolHCID 887—
ProductTert-butyl (2-fluoro-5-hydroxyphenyl)carbamateHCID 5774938599.3%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 3-[(tert-butoxycarbonyl)amino]-4-fluorophenyl tert-butyl carbonate (33.1 g, 101 mmol), sodium methoxide (6.55 g, 121 mmol) and methanol (500 mL) was stirred at 40° C. for 15 hr. The reaction mixture was concentrated under reduced pressure, and ethyl acetate and water were added to the residue. The organic layer was separated, washed with water and saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, and the residue was dried to give the title compound (22.8 g, quant.) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304557B2
Source datasetuspto-grants-2012_11
ORD IDord-cf2dacc1405241a0bb8b39f087e67222
Source noteuspto-grants-2012_11