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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292064Generated: October 31, 2026

Ethanethiol → HCID 14307643, compound

https://huagongshe.com/reaction/2292064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantHCID 14257811HCID 14257811—
SolventMethanolHCID 887—
ProductHCID 14307643HCID 14307643—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 2-(4-methoxybenzyl)-3-methyl-5-propyl-4,7-benzofurandione (from Preparation 28) (0.988 g, 3.05 mmol) in MeOH (23 mL) was added ethanethiol (2.5 mL). After a few minutes, the yellow quinone passed into solution giving a reddish colour. The reaction was cooled to 0° C. and solid FeCl3 (2.5g) was added. The reaction was quenched 10% HCl and extraction with CH2Cl2 afforded the crude product which was chromatographed on silica gel (5% EtOAc/hexane) to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04800228
Source datasetuspto-grants-1989_01
ORD IDord-b8d1945098554e4c9bb9f3c7a8e0a58d
Source noteuspto-grants-1989_01