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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059179Generated: November 2, 2026

Triethylamine → HCID 57077393, compound

https://huagongshe.com/reaction/2059179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant7-Bromo-4-hydroxy-2,3-dihydro-1H-inden-1-oneHCID 20545961—
ReactantHCID 131712694HCID 131712694—
SolventTolueneHCID 1140—
ProductHCID 57077393HCID 57077393—

Reaction Conditions

Temperature0 °C

Reaction Steps

S-Ethyl O-(3-methylthiophenyl) chlorothiophosphate (0.015 mole) dissolved in dry toluene (80) is charged into a glass reaction vessel equipped with a stirrer, thermometer and gas inlet tube. The solution is cooled to about 0° C. and a solution of 7-bromo-4-hydroxyindan-1-one (0.015 mole) and triethylamine (0.0175 mole) in toluene (20 ml) is slowly added with stirring. After the addition is completed the reaction mixture is allowed to warm to room temperature and stirring is continued for a period of about 8 hours. After this time the reaction mixture is filtered and the filtrate is washed with water. The washed solution is then dried and is stripped of solvent leaving a residue. This residue is chromatographed through a 200 ml clay column using ethyl acetate and hexane mixtures as the eluant. Ten separate fractions each containing increasing percentages of ethyl acetate are collected and analyzed by IR for the product. The appropriate fractions are then combined stripped of solvent and subjected to vacuum to yield the desired product S-ethyl O-(3-methylthiophenyl) O-(7-bromoindan-1-on-4-yl) thiophosphate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04322414
Source datasetuspto-grants-1982_03
ORD IDord-4daf94c4970848538a5da3d3a15ccede
Source noteuspto-grants-1982_03