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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763811Generated: November 2, 2026

Phosphorus oxychloride → HCID 70615283, compound

https://huagongshe.com/reaction/1763811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 88801791HCID 88801791—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 70615283HCID 70615283—

Reaction Steps

Phosphorus oxychloride (0.5 ml. 5.47 mmole) was added dropwise over 3 min. to a stirred suspension of 2,2,2-trichloroethyl 7β-formamido-3-methylthiomethylceph-3-em-4-carboxylate (1.05 g., 2.5 mmole) in dry methanol (10 ml.). During the addition the starting material went into solution and the temperature of the mixture reached a maximum of ca.45°. After 1 min. a white solid came out of solution and the mixture rapidly set solid. The mixture was diluted with ether (10 ml.), stirred briefly and the product collected, washed with ether (ca. 25 ml.) and dried to furnish the title hydrochloride as a feathery white solid (941 mg., 88%), m.p. 169° to 172° (dec.) [α]D + 5.25°, λmax. (MeOH) 272.5 nm. (ε 6,640), νmax. ca. 2600 (N+H3), 1775 (azetidin-2-one) and 1720 cm-1 (CO2CH2CCl3), τ 4.69 (1H,d, J 5 Hz; C7 -H), 4.88 and 5.01 (2H,AB-q, J 12 Hz; CH2CCl3), 4.90 (1H,d, J 5 Hz; C6 -H), 6.14 and 6.39 (2H,AB-q,J17 Hz C2 -CH2), 6.23 (2H,s; CH2SCH3) and 7.97 (3H,s; SCH3) (Found: C, 31.2; H, 3.3; Cl, 33.0; N, 6.6; S, 15.0. C11H 14 Cl4N2O3S2 (428.2) requires C, 30.85, H, 3.3; Cl, 33.1; N, 6.55; S, 15.0%). Electrophoresis showed a single spot, RX 1.56 (X=cephalexin) which migrated towards the cathode and which gave a mauve colour upon spraying with 0.5% (W/V) ninhydrin in ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04113591
Source datasetuspto-grants-1978_09
ORD IDord-0e5692239064417c83e633ebadd796e4
Source noteuspto-grants-1978_09