Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286406Generated: October 31, 2026

4-Fluorothiophenol → HCID 23462885, compound

https://huagongshe.com/reaction/2286406

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorothiophenolHCID 67789—
ReactantHCID 12668031HCID 12668031—
SolventMethanolHCID 887—
ProductHCID 23462885HCID 23462885—

Reaction Steps

To a solution of 1.0 g. (0.0078 mole) of p-fluorothiophenol in 200 ml. of methanol was added portionwise 2 g. (0.0073 mole) of 3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-dione hydrobromide (prepared as in Example 2) and the resulting mixture was stirred at room temperature under argon for 1 hour. The methanol was distilled from the reaction mixture in vacuo and the residue was partitioned between ether and water. The aqueous layer was extracted with ether and then made basic with ammonium hydroxide solution. The precipitate was filtered and the dried filtrate was chromatographed on silica using methanol/chloroform. The material eluted from the column was slurried with ether and filtered. Distillation of the ether gave 7,8-dihydroxy-6-(p-fluorophenylthio)-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine, m.p. 164°-166° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04265890
Source datasetuspto-grants-1981_05
ORD IDord-6ecba91589b74ad589616d81ef7f8f78
Source noteuspto-grants-1981_05