HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653563Generated: October 29, 2026
N,N-Dimethylaniline → HCID 141560563, compound
https://huagongshe.com/reaction/653563
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 20194650 | HCID 20194650 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 141560563 | HCID 141560563 | — |
Reaction Steps
1.82 g (2.62 mmol) of [(Z)-2-(1-benzhydryloxycarbonyl-1-cyclobutoxyimino)-2-(2-tritylaminothiazol-4-yl)acetic acid and 1.09 g (2.62 mmol) of benzhydryl 7-amino-3-chloromethyl-3-cephem-4-carboxylate were dissolved in 40 ml of methylene chloride, and then 1.06 ml (8.39 mmol) of N,N-dimethylaniline and 0.26 ml (2.75 mmol) of phosphorus oxychloride were dropwise added thereto under cooling with ice. The mixture was stirred at the same temperature for 4 hours. To the reaction solution, 30 ml of chloroform and 30 ml of water were added. 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 a residue of the above-identified compound. The residue of the compound thus obtained was employed for the next reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04677100 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-d03d25a2fd50458cbfcbd50ae242347e |
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| Source note | uspto-grants-1987_06 |
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