HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132016Generated: October 28, 2026
Acetic Anhydride → HCID 67046148, compound
https://huagongshe.com/reaction/132016
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Asimadoline hydrochloride | HCID 9846614 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 67046148 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07385065B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-4b623baaa60b418d985299f04a3aa531 |
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| Source note | uspto-grants-2008_06 |
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