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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979620Generated: October 29, 2026

Boric Acid → 7-Amino-3-acetylthiomethyl-ceph-3-eme-4-carboxylic acid

https://huagongshe.com/reaction/1979620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoric AcidHCID 7628—
Reactant7-Aminocephalosporanic acidHCID 441328—
ReactantHCID 178418634HCID 178418634—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
Product7-Amino-3-acetylthiomethyl-ceph-3-eme-4-carboxylic acidHCID 8860088877%

Reaction Conditions

Temperature75 °C

Reaction Steps

56.8 ml (0.8 mole) of thioacetic acid and 140 ml (1.0 mole) of triethylamine were added successively to three liters of water under stirring. The homogenous mixture was heated to 75° C. and there were added in one shot 100.0 g (0.368 mole) of 7-aminocephalosporanic acid (90%), causing a pH variation from 9.05 to 5.03. Thereafter there were added, first, 20 to 21 ml of triethylamine until a solution was formed and then 61.0 g of boric acid. Stirring was continued at 70° C. for 60 minutes and the reaction isoelectric pH was checked, regulating the variation from 5.80 to 5.60 by gradual addition of 10.9 ml of thioacetic acid over a period of about 30 minutes. During the last 15 minutes, the pH varied to a virtually constant value of 5.70. The precipitation increased during the reaction and was completed at 60° C. and the pH was adjusted to 4.80 (25° C.) by the addition of about 300 ml of 1N hydrochloric acid. The solid was filtered, washed successively with water and acetone to give 73.5 g of the compound of the title, with a 77% yield. It turned brown at about 215° C. and decomposed at 228° C. (polarised light). The excess thioacetic acid was recovered from the mother liquors at pH 1.0 by extraction with an organic solvent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04481357
Source datasetuspto-grants-1984_11
ORD IDord-812465f7eafb4d8fbb462665647b9f84
Source noteuspto-grants-1984_11