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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992677Generated: October 31, 2026

Acetic Acid → Methyl (3S,4R)-4-(2,4-difluorophenyl)-1-isopropylpyrrolidine-3-carboxylate

https://huagongshe.com/reaction/1992677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetoneHCID 180—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactantmethyl (3S,4R)-4-(2,4-difluorophenyl)pyrrolidine-3-carboxylateHCID 59130986—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
ProductMethyl (3S,4R)-4-(2,4-difluorophenyl)-1-isopropylpyrrolidine-3-carboxylateHCID 59130981—

Reaction Steps

Sodium triacetoxyborohydride (1.32 g, 6.22 mmol) and acetic acid (235 μL, 4.14 mmol) were added to a solution of acetone (304 μL, 4.14 mmol) and methyl (3S,4R)-4-(2,4-difluorophenyl)pyrrolidine-3-carboxylate, from preparation 31 (1 g, 4.14 mmol) in dichloromethane (20 mL) at room temperature. The resulting mixture was stirred for 2 hours and diluted with dichloromethane (10 mL). Aqueous sodium hydrogen carbonate solution was added (2×20 mL) followed by brine (20 mL). The phases were separated, the organic phase was dried over magnesium sulfate, filtered and the solvent was removed in vacuo to give the crude residue. Purification of the residue by column chromatography using dichloromethane:methanol (99:1-98:2) as eluent afforded the desired product, 1.01 g (86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07649002B2
Source datasetuspto-grants-2010_01
ORD IDord-2e16f5cf4a8a4818b8784bfc91aa6392
Source noteuspto-grants-2010_01