HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731711Generated: November 2, 2026
m-Chloroperbenzoic acid → HCID 54410203, compound
https://huagongshe.com/reaction/1731711
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 54407251 | HCID 54407251 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 54410203 | HCID 54410203 | 73.7% |
Reaction Steps
A solution of meta-chloroperbenzoic acid (85% pure) (0.05 g) in methylene chloride (1 cc) is added all at once to a solution, cooled to -10° C., of product (8b) (0.2 g) in methylene chloride (5 cc). After 30 minutes at -10° C., the reaction mixture is diluted with ethyl acetate (20 cc) and washed with a saturated solution of sodium bicarbonate (2×10 cc) and a saturated solution of sodium chloride (2×10 cc). After the mixture has been dried over sodium sulphate and concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 30° C., crude syn isomer of 2-benzhydryloxycarbonyl-3-(2,2-dichloroethyl)-7-[2-methoxyimino-2-(2-tritylaminothiazol-4-yl)-acetamido]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-5-oxide (product 8) (0.15 g) is obtained in the form of a hard orange foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04622393 |
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| Source dataset | uspto-grants-1986_11 |
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| ORD ID | ord-c798c2c7a372428a8a6429a72d87e127 |
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| Source note | uspto-grants-1986_11 |
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