HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904996Generated: November 1, 2026
Ammonium Chloride → HCID 67743997, compound
https://huagongshe.com/reaction/904996
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 11024808 | HCID 11024808 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Magnesium Chloride | HCID 5360315 | — |
| Product | HCID 67743997 | HCID 67743997 | — |
Reaction Steps
Methyl magnesium chloride (2.9 ml, of 2.9 M in tetrahydrofuran) was added to a solution of 500 mg (3R-trans)-3-phenoxyacetylamino-4-phenylsulfonyl-2-azetidinone in 11.1 ml of 0.5 M magnesium dichloride in tetrahydrofuran under nitrogen and chilled in an ice/acetone bath (-10° C.). After 2 hours, the mixture was added to saturated aqueous ammonium chloride and extracted with ethyl acetate. The extract was washed with water, dried over sodium sulfate, and evaporated. Treatment of the residue with dichloromethane/ethyl ether gave 106 mg of cis-3-phenoxyacetylamino-4-methyl-2-azetidinone. The corresponding trans isomer, as well as some cis isomer, was present in the mother liquor, as shown by NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04421686 |
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| Source dataset | uspto-grants-1983_12 |
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| ORD ID | ord-0367e442cc00439494c7e41159036afa |
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| Source note | uspto-grants-1983_12 |
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