HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388959Generated: October 30, 2026
N,N-Dimethylaniline → HCID 131711216, compound
https://huagongshe.com/reaction/1388959
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Dichlorodimethylsilane | HCID 6398 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | 7beta-Phenoxyacetamido-3-methoxy-3-cephem-4-carboxylic acid | HCID 12784142 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 131711216 | HCID 131711216 | — |
Reaction Steps
(ci) A suspension of 11.75 g of 93 percent strength (corresponding to 10.93 g of 100% strength) of 7β-phenoxyacetamido-3-methoxy-ceph-3-em-4-carboxylic acid and 13.4 ml (12.73 g) of N,N-dimethylaniline in 47 ml of absolute methylene chloride (distilled over P2O5) is treated, at +20° C., under nitrogen, with 3.6 ml (3.87 g) of dimethyldichlorosilane and the mixture is then stirred for 30 minutes at the same temperature. The solution, which is now clear, is cooled to -18°/-19° and 7.8 g of solid phosphorus pentachloride are added, the internal temperature rising to -10°. After stirring for 30 minutes in a bath at -20°, the clear solution is added dropwise, in the course of about 7 minutes, to a mixture, cooled to -20°, of 47 ml of n-butanol (anhydrous, dried over Sikkan) and 4.4 ml (4.18 g) of dimethylaniline. The internal temperature rises to -8°. The mixture is stirred for a further 30 minutes, initially in a bath at -20° and subsequently in an ice bath (0°), so that a final internal temperature of -10° is reached. A mixture of 47 ml of dioxane and 1.6 ml of water is added dropwise at this temperature (time taken, about 5 minutes). The product thereupon crystallises out slowly. After stirring for a further 10 minutes, the pH of the mixture, in an ice bath, is brought to a value of between 2.2 and 2.4, and kept at this value, by adding about 9.5 ml of tri-n-butylamine, in portions, in the course of about 1 hour (the first 3 ml are added in the first 5 minutes). The product is then filtered off, washed, in portions, with about 30 ml of dioxane and then with about 15 ml of methylene chloride and crystalline 7β-amino-3-methoxy-ceph-3-em-4-carboxylic acid hydrochloride dioxanate is thus obtained; melting point above 300° C.; UV spectrum (in 0.1 N sodium bicarbonate): λmax =270 mμ (ε=7,600); IR spectrum (nujol): characteristic bands at 5.62; 5.80; 5.88; 6.26; 6.55; 7.03; 7.45; 7.72; 7.96; 8.14; 8.26; 8.45; 8.64; 8.97; 9.29; 10.40 and 11.47 mμ; [α]D20 =+134°±1° (c=1; 0.5 N sodium bicarbonate solution).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04434287 |
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| Source dataset | uspto-grants-1984_02 |
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| ORD ID | ord-98c2a93b9e0349868f8b450825d38cfa |
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| Source note | uspto-grants-1984_02 |
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