Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370613Generated: October 28, 2026

2-Aminothiophenol → HCID 4575136, compound

https://huagongshe.com/reaction/370613

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
ReactantSodium HydroxideHCID 14798—
Reactant2-Bromoethyl methyl etherHCID 80972—
SolventEthanolHCID 702—
ProductHCID 4575136HCID 457513689%

Reaction Steps

To a solution of 2-aminothiophenol (93%, 123 g, 0.910 mol) and sodium hydroxide (40.2 g, 1.00 mol) in 90% aqueous ethanol (637 ml) was added dropwise 2-bromoethylmethylether (127 g, 0.910 mol) at room temperature. When the addition was complete, the reaction mixture was refluxed for 2 hours, cooled to room temperature, and then concentrated in vacuo. The resulting residue was diluted with water (1400 ml) and extracted with methylene chloride (3×500 ml). The extracts were washed with water (2×500 ml) and brine (500 ml), dried with (MgSO4), filtered and concentrated to give a dark oil. Distillation of the crude product gave 2-(2-methoxyethylthio)benzenamine (148 g, 89%) as a light yellow oil; bp 90°-103° (0.1 mm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04528024
Source datasetuspto-grants-1985_07
ORD IDord-c57de50505eb4c19b657273785d5b9bd
Source noteuspto-grants-1985_07