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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050981Generated: November 1, 2026

Ethylparaben → Ethyl 4-(4,4-dimethyl-6-thiochromanoyloxy)benzoate

https://huagongshe.com/reaction/2050981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylparabenHCID 8434—
ReactantTriethylamineHCID 8471—
Reactant4,4-Dimethyl-3,4-dihydro-2H-1-benzothiopyran-6-carboxylic acidHCID 19834228—
SolventChloroformHCID 6212—
ProductEthyl 4-(4,4-dimethyl-6-thiochromanoyloxy)benzoateHCID 19834227—

Reaction Steps

A solution of 280 mg (1.26 mmol) of 4,4-dimethyl-6-carboxythiochroman and 252 mg (2.52 mmol) of triethylamine in 15 ml of chloroform was stirred at room temperature for 0.5 hours and then treated with 481 mg (1.26 mmol) of bias(2-oxo-3-oxazolidinyl)phosphinic chloride. The reaction mixture was stirred for 0.5 h, treated with 209 mg (1.26 mmol) of ethyl 4-hydroxybenzoate and then stirred at room temperature for a further 12 hours. The reaction mixture was washed successively with dilute HCl and saturated sodium bicarbonate solutions. The organic layer was concentrated in-vacuo and the resultant crude product purified by flash chromatography (silica; 10% ethyl acetate in hexane) followed by reversed-phase high pressure liquid chromatography (Whatman Partisil M20 10/50 ODS-2; 10% water in acetonitrile) to give the title compound as a colorless oil. PMR (CDCl3): δ1.38 (6H, s), 1.42 (3H, t, J~7.0 Hz), 1.98 (2H, m), 3.07 (2H, m), 4.39 (2H, q, J~7.0 Hz), 7.20 (1H, d, J~9.0 Hz), 7.28 (2H, d, J~8.1 Hz), 7.82 (1H, dd, J~9.0, 1.8 Hz), 8.12 (2H, d, J~8.1 Hz), 8.17 (1H, d, J~1.8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05015658
Source datasetuspto-grants-1991_05
ORD IDord-7eb71e1c9640480d8da446c5e8ee93c1
Source noteuspto-grants-1991_05