HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484037Generated: October 30, 2026
Phenylacetyl chloride → HCID 14543802, compound
https://huagongshe.com/reaction/484037
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Ethyl oxoacetate | HCID 70211 | — |
| Reactant | HCID 20086945 | HCID 20086945 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 14543802 | HCID 14543802 | — |
Reaction Steps
To a solution of 17 ml of triethylamine and 5.0 g of the imine formed from ethyl glyoxalate and p-anisidine in 100 ml of refluxing 1,2-dichloroethane was added dropwise over 2 hours a solution of 16 ml of freshly distilled phenylacetyl chloride in 50 ml of dichloroethane. After refluxing for three hours the reaction was worked-up as per the 3-azidoazetidinone. The crude residue was chromatographed to yield the cis and trans isomers of 4-carboethoxy-1-(p-methoxyphenyl)-3-phenylazetidin-2-one as oils; cis: NMR (CDCl3): δ 7.2 (m, 7H), 6.7 (d, J=9, 2H), 4.7 (s, 2H), 3.6 (s, 3H), 3.6 (q, J=7, 2H), 0.7 (t, J=7, 3H); trans: NMR (CDCl3): δ 7.3 (m, 7H), 6.8 (d, J=9, 2H), 4.5 (d, J=2, 1H), 4.45 (d, J=2, 1H), 4.1 (q, J=7, 2H), 3.6 (s, 3H), 1.2 (t, J=7, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05229381 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-29fd0eca41774ab8a1f0e04c420c4f67 |
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| Source note | uspto-grants-1993_07 |
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