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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660980Generated: October 25, 2026

Triethylamine → dimethyl-thiocarbamic acid O-(4'-tert-butyl-2,6-dimethyl-biphenyl-4-yl)ester

https://huagongshe.com/reaction/660980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDimethylthiocarbamoyl chlorideHCID 27871—
Reactant4'-Tert-butyl-2,6-dimethylbiphenyl-4-OLHCID 53302018—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,4-DioxaneHCID 31275—
Productdimethyl-thiocarbamic acid O-(4'-tert-butyl-2,6-dimethyl-biphenyl-4-yl)esterHCID 8662517195.8%

Reaction Steps

To a solution of 4′-tert-butyl-2,6-dimethyl-biphenyl-4-ol (10 g, 37.3 mmol) in dioxane (157 ml) is added 4-dimethylaminopyridine (476 mg, 3.9 mmol), triethylamine (10 mL, 78.6 mmol), and dimethylthiocarbamoyl chloride (6.1 g, 49.1 mmol). The reaction mixture is heated to reflux overnight. After cooling to rt, the reaction mixture is partitioned between ethyl acetate and water. The aqueous layer is back-extracted with ethyl acetate, and the combined organic layers are dried and concentrated. The resulting residue is applied to silica gel and eluted using 20% ethyl acetate in hexanes to give dimethyl-thiocarbamic acid O-(4′-tert-butyl-2,6-dimethyl-biphenyl-4-yl)ester (12.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084489B2
Source datasetuspto-grants-2011_12
ORD IDord-9cb85568414d4ae69079bd087558d3c0
Source noteuspto-grants-2011_12