HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375499Generated: October 29, 2026
Phenylacetyl chloride → HCID 67745344, compound
https://huagongshe.com/reaction/375499
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 67745321 | HCID 67745321 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67745344 | HCID 67745344 | — |
Reaction Steps
0.35 cm3 of triethylamine and a solution of 0.17 cm3 of phenylacetyl chloride in 5 cm3 of dichloromethane are added to a suspension, cooled to 0° C., of 0.46 g of (4aRS,7aRS)-4,4-diphenylperhydrothiopyrano[2,3-c]pyrrole 1,1-dioxide hydrochloride in 10 cm3 of dichloromethane. After stirring for 1 hour at 0° C. and then 1 hour at 20° C., the reaction mixture is diluted with 10 cm3 of dichloromethane, washed twice with 30 cm3 of distilled water, dried over magnesium sulphate and concentrated to dryness under reduced pressure (2.7 kPa). The oil obtained is crystallized from 30 cm3 of ethyl ether, the crystals are drained and dried. 0.50 g of (4aRS,7aRS)-4,4-diphenyl-6-phenylacetylperhydrothiopyrano[2,3-c]pyrrole 1,1-dioxide is obtained in the form of white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05484942 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-5b921a9a8cf4413db855e3bccb227e8f |
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| Source note | uspto-grants-1996_01 |
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