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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279939Generated: October 30, 2026

Benzyl chloroformate → HCID 118117725, compound

https://huagongshe.com/reaction/2279939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 68712100HCID 68712100—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 118117725HCID 11811772556%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 2-amino-2-(3-(benzyloxy)phenyl)acetate (1.09 g, 4 mmol) in a mixture of tetrahydrofuran and water (1:1, 90 mL) at 0° C. was added benzyl chloroformate (0.57 mL, 4 mmol) and aqueous sodium hydroxide (4 N, 1 mL, 4 mmol) simultaneously. The mixture was stirred at 0° C. for one hour. The ice bath was removed and the reaction mixture was stirred at room temperature for 16 h. The solvent was removed in vacuo and ethyl acetate (100 mL) and water (30 mL) were added. The layers were separated and the aqueous phase re-extracted with ethyl acetate (2×50 mL). The combined organic fractions were dried over magnesium sulfate, filtered and the solvent removed in vacuo. The residue was purified by silica gel column chromatography, eluting with 0-40% ethyl acetate in iso-hexane to afford the title compound (900 mg, 56%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133185B2
Source datasetuspto-grants-2015_09
ORD IDord-9193e5fd8a8d4e1c963cbcd056c035d2
Source noteuspto-grants-2015_09