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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132016Generated: October 28, 2026

Acetic Anhydride → HCID 67046148, compound

https://huagongshe.com/reaction/132016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantAsimadoline hydrochlorideHCID 9846614—
SolventTriethylamineHCID 8471—
ProductHCID 67046148HCID 67046148—

Reaction Steps

30 ml of acetic anhydride and 15 ml of triethylamine are added to 5.0 grams (11.0 mmol) of N-methyl-N-[(1S)-1-phenyl-2-((3S)-3-hydroxy-pyrrolidin-1-yl)ethyl]-2,2-diphenylacetamide, hydrochloride, and the mixture is heated for two hours on a steam bath. The reaction mixture is subsequently evaporated to dryness, and the residue is taken up in ether and washed with bicarbonate solution. The organic phase is subsequently dried, and the solvent is distilled off. The resultant residue is purified by column chromatography on silica gel with diethyl ether/methanol (99:1) as eluent. The resultant crude product of N-{2-[(3S)-3-acetoxy-1-pyrrolidinyl]-(1S)-1-phenylethyl}-2,2-diphenyl-N-methylacetamide can be purified further by taking up in diethyl ether, precipitation by addition of ethereal HCl, filtering-off of the resultant crystals under reduced pressure, washing of the crystals with ether and drying in air (Rf=0.6 (TLC on silica gel 6 F254 with dichloromethane/methanol (8:2) as eluent)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07385065B2
Source datasetuspto-grants-2008_06
ORD IDord-4b623baaa60b418d985299f04a3aa531
Source noteuspto-grants-2008_06