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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694925Generated: November 2, 2026

Acetic Acid → [2-(2,6-Difluorophenylamino)-1,1-dimethylethyl]carbamic acid t-butyl ester

https://huagongshe.com/reaction/1694925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2,6-DifluoroanilineHCID 79647—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-butyl N-(2-methyl-1-oxopropan-2-yl)carbamateHCID 14578674—
SolventDichloromethaneHCID 6344—
Product[2-(2,6-Difluorophenylamino)-1,1-dimethylethyl]carbamic acid t-butyl esterHCID 6664588731%

Reaction Steps

17.0 g of sodium triacetoxyborohydride (80.0 mmol) was added to a solution of 15.0 g of (1,1-dimethyl-2-oxoethyl)carbamic acid t-butyl ester obtained in Reference Example 3 (80.0 mmol), 5.16 g of 2,6-difluoroaniline (40.0 mmol) and 2.09 ml of acetic acid (40.0 mmol) in methylene chloride (400 ml) under ice-cooling, and the mixture was stirred at room temperature for 19 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=20/1-10/1) to obtain 3.68 g of the title compound (yield: 31%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158790B2
Source datasetuspto-grants-2012_04
ORD IDord-e048b06f9d9948819d12e8135d57b6c5
Source noteuspto-grants-2012_04