HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029948Generated: October 30, 2026
Phenylacetyl chloride → HCID 67916020, compound
https://huagongshe.com/reaction/1029948
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 67915919 | HCID 67915919 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67916020 | HCID 67916020 | 20.2% |
Reaction Steps
A suspension of (3aRS,7aRS)-7,7-bis-(3-tolyl)-4-perhydroisoindolone hydrochloride (1.5 g) in dichloromethane (30 cc) cooled to +4° C. is treated with triethylamine (1.15 cc) and then with phenylacetyl chloride (0.63 g). The reaction mixture is stirred for 5 hours at 25° C. and then washed with water (3×100 cc). The organic phase is dried over magnesium sulphate and filtered and the filtrate is concentrated to dryness under reduced pressure (2.7 kPa). The residue is crystallized twice from acetonitrile to give (3aRS,7aRS)-7,7-bis-(3-tolyl)-2-(phenylacetyl)-4-perhydroisoindolone (0.36 g). m.p.=207° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05102667 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-d9e78980a31749f582720bbe11a8cc45 |
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| Source note | uspto-grants-1992_04 |
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