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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701165Generated: October 31, 2026

Diazomethane → HCID 53703941, compound

https://huagongshe.com/reaction/1701165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
ReactantHCID 20348737HCID 20348737—
SolventDiethyl EtherHCID 3283—
ProductHCID 53703941HCID 53703941—

Reaction Steps

A solution of 320 mgm (7.6 millimols) of diazomethane (prepared from 2.14 gm of p-toluenesulfonyl-methylnitrosoamide in 30 ml of ether and 0.4 gm of potassium hydroxide in 10 ml of 96% ethanol and subsequent distillation) was added, while stirring, to a suspension of 2.3 gm (7.5 millimols) of [1-(2'-fluoro-4-biphenylyl)-ethylsulfinyl]-acetic acid (m.p.: 164°-165° C.) in 20 ml of ether. The acid dissolved, accompanied by nitrogen evolution. After the reaction was finished, the mixture was evaporated, and the residue was recrystallized from benzene cyclohexane (1/5). Yield: 2.0 gm (83.5% of theory); m.p.: 75°-77° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04191776
Source datasetuspto-grants-1980_03
ORD IDord-14faa6a3bc1d4363ad7a4831f307724a
Source noteuspto-grants-1980_03