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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127462Generated: October 30, 2026

tert-Butanol → HCID 131711476, compound

https://huagongshe.com/reaction/127462

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantHCID 14197971HCID 14197971—
Reactant2-[4-(Benzthiazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methoxy-isocrotonic acid chlorideHCID 88757915—
SolventDichloromethaneHCID 6344—
ProductHCID 131711476HCID 131711476—

Reaction Steps

A solution of 266 mg (0.5 mM) of a crude mixture consisting of 2-[4-benzthiazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methoxy-crotonic acid chloride and 2-[4-(benzthiazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methoxy-isocrotonic acid chloride in 5 ml of dry methylene chloride is added dropwise over the course of 15 minutes at 0° C., whilst stirring, to a solution of 0.10 ml of triethylamine in 0.5 ml of dry tert.-butanol and 3 ml of methylene chloride. After a further 15 minutes stirring, the reaction mixture is diluted with methylene chloride, washed with water, with dilute hydrochloric acid and again with water, dried over sodium sulphate and concentrated by evaporation in vacuo. The residue is chromatographed on 10 g of acid-washed silica gel, using toluene/ethyl acetate (4:1) as the running agent. 7β-Phenoxyacetamido-3-methoxy-ceph-2-em-4-carboxylic acid tert.butyl ester is obtained. IR spectrum (in CH2Cl2): characteristic bands at 5.60, 5.77, 5.90 and 8.29μ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04255328
Source datasetuspto-grants-1981_03
ORD IDord-47790c3239e44a03b3027f651ee3603d
Source noteuspto-grants-1981_03