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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595456Generated: October 27, 2026

2-Mercaptoethanol → 2-[Methyl-bis(2-sulfanylethoxy) silyl]oxyethanethiol

https://huagongshe.com/reaction/595456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MercaptoethanolHCID 1567—
ReactantTriethylamineHCID 8471—
ReactantCID 71317501HCID 71317501—
Reactant2-[Dimethyl(2-sulfanylethoxy)silyl]oxyethanethiolHCID 71602155—
SolventDiethyl EtherHCID 3283—
Product2-[Methyl-bis(2-sulfanylethoxy) silyl]oxyethanethiolHCID 86716163—

Reaction Steps

The 2-[methyl-bis(2-sulfanylethoxy) silyl]oxyethanethiol (2) was synthesized according to the same procedure as 2-[dimethyl(2-sulfanylethoxy)silyl]oxyethanethiol (1), using triethylamine (8.08 g, 0.080 mol), trichloromethylsilane (3.98 g, 0.027 mol), and 2-mercaptoethanol (6.24 g, 0.080 mol) in ether (400 mL). 2-[methyl-bis(2-sulfanylethoxy) silyl]oxyethanethiol (2) was obtained as a clear, colorless, foul-smelling liquid (6.81 g, 93.2%). The product was purified by distillation under reduced pressure and obtained as a clear, colorless, foul-smelling liquid (4.53 g, 62.0%), Bp=128-129° C. at 0.25 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09243006B2
Source datasetuspto-grants-2016_01
ORD IDord-5341e6b9cf204074905f1e81a924ea78
Source noteuspto-grants-2016_01