Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248607Generated: October 24, 2026

2-Mercaptoethanol → Ethanol, 2-[[(4-ethenylphenyl)methyl]thio]-

https://huagongshe.com/en/reaction/248607

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MercaptoethanolHCID 1567—
ReactantPotassium HydroxideHCID 14797—
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
Reactantp-Vinylbenzyl chlorideHCID 74126—
SolventEthanolHCID 702—
ProductEthanol, 2-[[(4-ethenylphenyl)methyl]thio]-HCID 1469279885%

Reaction Steps

To a solution of potassium hydroxide (86 g, 1.3 moles) and 2,6-di-tert-butyl-p-cresol (1 g) in ethanol (1 liter) at room temperature was added under nitrogen atmosphere 2-mercaptoethanol (100 g, 1.3 moles), over fifteen minutes. Following addition the solution was stirred an additional hour at room temperature and then p-vinylbenzyl chloride (198 g, 1.3 moles) was added at room temperature over one hour. After addition, the mixture was allowed to reach ambient temperature overnight. The mixture was filtered and the solvent removed on a rotary evaporator. To the residue was added dichloromethane (1.2 liter) and the solvent was washed with water (3×200 ml), then with saturated NaCl solution (200 ml), dried over anhydrous magnesium sulfate, filtered and the solvent removed on a rotary evaporator. To the residue was added diethyl ether (200 ml) and petroleum ether (800 ml). The product crystallized and was then filtered to give a white solid: m.p. of 44°-45.5° C. Yield of 85%. Analysis calculated for C11H14OS: C. 68.0, H, 7.26, S, 16.50. Found: C, 67.7, H, 6.98, S, 15.37.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05210289
Source datasetuspto-grants-1993_05
ORD IDord-a6799965982b4b4484729b3c3149fb1c
Source noteuspto-grants-1993_05