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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694929Generated: October 26, 2026

Acetic Acid → HCID 66645618, compound

https://huagongshe.com/reaction/1694929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Chloro-5-fluoroanilineHCID 2736509—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-butyl N-(2-methyl-1-oxopropan-2-yl)carbamateHCID 14578674—
SolventDichloromethaneHCID 6344—
ProductHCID 66645618HCID 6664561853%

Reaction Steps

10.0 g of sodium triacetoxyborohydride (47.2 mmol) was added to a solution of 6.0 g of (1,1-dimethyl-2-oxoethyl)carbamic acid t-butyl ester obtained in Reference Example 3 (32.0 mmol), 4.6 g of 2-chloro-5-fluoroaniline (32.0 mmol) and 1.8 ml of acetic acid (32.0 mmol) in methylene chloride (320 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 5.36 g of the title compound (yield: 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158790B2
Source datasetuspto-grants-2012_04
ORD IDord-a3158525432b43c59e411a0debb53de4
Source noteuspto-grants-2012_04