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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388959Generated: October 30, 2026

N,N-Dimethylaniline → HCID 131711216, compound

https://huagongshe.com/reaction/1388959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantWaterHCID 962—
ReactantDichlorodimethylsilaneHCID 6398—
ReactantPhosphorus pentachlorideHCID 24819—
Reactant7beta-Phenoxyacetamido-3-methoxy-3-cephem-4-carboxylic acidHCID 12784142—
Solvent1-ButanolHCID 263—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 131711216HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04434287
Source datasetuspto-grants-1984_02
ORD IDord-98c2a93b9e0349868f8b450825d38cfa
Source noteuspto-grants-1984_02