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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171605Generated: November 2, 2026

Acetone → HCID 68766782, compound

https://huagongshe.com/reaction/1171605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium HydroxideHCID 14798—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 68769573HCID 68769573—
SolventDichloromethaneHCID 6344—
ProductHCID 68766782HCID 6876678299.1%

Reaction Steps

(3R,4S)-Methyl 4-((3S)-3-(benzyloxycarbonylamino)-2-oxopyrrolidin-1-yl)piperidine-3-carboxylate (1.00 g, 2.66 mmol, 1 eq.), sodium triacetoxyborohydride (0.85 g, 4.00 mmol, 1.5 eq.) and acetone (0.59 mL, 7.99 mmol, 3 eq.) were mixed in methylene chloride (15 mL) and stirred for 20 hours at room temperature. Worked up by adding 20 mL of 1.000 N NaOH. Stirred 10 minutes then extracted 3 times with methylene chloride. The organic layers were combined, dried over sodium sulfate and stripped to give methyl 4-((3S)-3-(benzyloxycarbonylamino)-2-oxopyrrolidin-1-yl)-1-isopropyl-piperidine-3-carboxylate (1.10 g) of a white glass. Yield=99%. LCMS detects (M+H)+=418.41.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829571B2
Source datasetuspto-grants-2010_11
ORD IDord-27bcc5d596ae41f7a783640b1538a59d
Source noteuspto-grants-2010_11