Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694902Generated: October 30, 2026

Acetic Acid → [2-(2-Benzyloxyphenylamino)-1,1-dimethylethyl]carbamic acid t-butyl ester

https://huagongshe.com/reaction/1694902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-BenzyloxyanilineHCID 240548—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-butyl N-(2-methyl-1-oxopropan-2-yl)carbamateHCID 14578674—
SolventDichloromethaneHCID 6344—
Product[2-(2-Benzyloxyphenylamino)-1,1-dimethylethyl]carbamic acid t-butyl esterHCID 6664595691.8%

Reaction Steps

6.38 g of sodium triacetoxyborohydride (30.1 mmol) was added to a solution of 4.68 g of (1,1-dimethyl-2-oxoethyl)carbamic acid t-butyl ester obtained in Reference Example 3 (25.0 mmol), 5.0 g of 2-benzyloxyaniline (25.0 mmol) and 1.44 ml of acetic acid (25.0 mmol) in methylene chloride (250 ml) under ice-cooling, and the mixture was stirred at room temperature for 16 hours. A saturated sodium bicarbonate aqueous solution was added to the reaction mixture, followed by extraction with methylene chloride. Then, the organic layer was washed with brine and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (elution solvent:hexane/ethyl acetate=5/1) to obtain 8.50 g of the title compound (yield: 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158790B2
Source datasetuspto-grants-2012_04
ORD IDord-50ba56b8b8574819a2106f66ca9228b4
Source noteuspto-grants-2012_04