HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252313Generated: October 29, 2026
N,N-Dimethylaniline → HCID 178525023, compound
https://huagongshe.com/reaction/1252313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Benzhydryl 7-Amino-3-chloromethyl-3-cephem-4-carboxylate | HCID 13239626 | — |
| Reactant | HCID 21269519 | HCID 21269519 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178525023 | HCID 178525023 | — |
Reaction Steps
2.12 g (3 mmol) of (Z)-2-(1-benzhydryloxycarbonyl-1-cyclopentyloxyimino)-2-(2-tritylaminothiazol-4-yl) acetic acid and 1.24 g (3 mmol) of benzhydryl 7-amino-3-chloromethyl-3-cephem-4-carboxylate were dissolved in 50 ml of methylene chloride, and 1.2 ml (9.6 mmol) of N,N-dimethylaniline was added under cooling with ice. Then, 0.29 ml (3.15 mmol) of phosphorus oxychloride was dropwise added thereto, and the mixture was stirred at the same temperature for 4 hours. 30 ml of chloroform and 30 ml of water was added to the reaction solution. The organic layer was washed with water and with a saturated sodium chloride aqueous solution, then dried over anhydrous sodium sulfate and concentrated to obtain the residue of the above identified compound, which was used for the subsequent reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04742053 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-4af7dd36e5344caa952f181e0911c29e |
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| Source note | uspto-grants-1988_05 |
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