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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246624Generated: October 30, 2026

Ethanethiol → 3-Methoxy-4-(methylsulfanyl)phenol

https://huagongshe.com/reaction/1246624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantDibenzyl etherHCID 7657—
ReactantBoron trifluoride etherateHCID 8000—
SolventDichloromethaneHCID 6344—
Product3-Methoxy-4-(methylsulfanyl)phenolHCID 2187713028%

Reaction Steps

The benzylether from stage (iii) (9.27 g, 39.5 mmol) was dissolved in DCM (5 mL), ethanethiol (5 mL) and BF3.OEt2 (5 mL, 39.5 mol) were then added at room temperature under a nitrogen atmosphere. The mixture was stirred overnight before the reaction was quenched with 2M HCl and stirred for a further 30 min. The mixture was then basified by the addition of 2M NaOH until pH 10 was attained. The mixture was then washed with EtOAc (3×50 mL). The aqueous layer was re-acidified by the addition of 2M HCl to pH 1 and extracted with EtOAc (4×50 mL). The extracts were combined, dried (MgSO4) and evaporated to an oil. Purification by flash chromatography [SiO2; EtOAc/pentane (1:9→1:4)] afforded the desired phenol compound as a colourless solid (1.73 g, 28%); δH (CDCl3, 400 MHz) 2.21 (3H, s), 3.70 (3H, s), 6.30 (1H, d), 6.35 (1H, s), 6.96 (1H, d), 9.39 (1H, brs).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129234B2
Source datasetuspto-grants-2006_10
ORD IDord-06e630104681478e9148516800170974
Source noteuspto-grants-2006_10