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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378810Generated: October 26, 2026

1,1-Ethanediol → 6-Bromo-5,8-dimethylspiro[thiochromane-4,2'-[1,3]dioxolane]

https://huagongshe.com/reaction/378810

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-EthanediolHCID 151211—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant5,8-Dimethyl-6-bromothiochroman-4-oneHCID 15278495—
SolventDiethyl EtherHCID 3283—
SolventTrimethyl orthoformateHCID 9005—
Product6-Bromo-5,8-dimethylspiro[thiochromane-4,2'-[1,3]dioxolane]HCID 21696593—

Reaction Conditions

Temperature80 °C

Reaction Steps

58.4 g (0.22 mol) of 6-bromo-5,8-dimethyl-4-thiochromanone were dissolved in 380 ml of trimethyl orthoformate, admixed with 555 g (8.9 mol) of ethanediol and 0.2 g of p-toluenesulfonic acid monohydrate and stirred at 80° C. overnight. The mixture was subsequently allowed to cool, diluted with 500 ml of diethyl ether and washed with a 1:1 mixture of 1 M aqueous sodium hydroxide solution and sat. NaCl solution (2×500 ml) and subsequently with sat. NaCl solution (300 ml). The organic phase was dried over MgSO4 and concentrated using a rotary evaporator. The residue was taken up in 50 ml of heptaneldiethyl ether (9:1) and stored in a cold place. The crystals which had precipitated overnight were filtered off with suction, washed with cold heptane and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06297196B1
Source datasetuspto-grants-2001_10
ORD IDord-2d9e3ecf9bc24abbbd3d7d581b9c76a4
Source noteuspto-grants-2001_10