HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246624Generated: October 30, 2026
Ethanethiol → 3-Methoxy-4-(methylsulfanyl)phenol
https://huagongshe.com/reaction/1246624
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Dibenzyl ether | HCID 7657 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Methoxy-4-(methylsulfanyl)phenol | HCID 21877130 | 28% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129234B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-06e630104681478e9148516800170974 |
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| Source note | uspto-grants-2006_10 |
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