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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935593Generated: October 31, 2026

2-(4-t-Butylphenoxy)thioacetamide → HCID 10134842, compound

https://huagongshe.com/reaction/1935593

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-t-Butylphenoxy)thioacetamideHCID 2743912—
Reactant2-Bromo-5-chloro-2,3-dihydro-1H-inden-1-oneHCID 11334069—
SolventAcetoneHCID 180—
ProductHCID 10134842HCID 10134842—

Reaction Steps

At room temperature, 0.49 g of 2-bromo-5-chlorindan-1-on and 0.45 g of 2-(4-tert-butylphenoxy)-thioacetamide were dissolved in 10 ml of dry acetone, and the mixture was stirred at room temperature for 12 h. The precipitated hydrobromide was filtered off with suction and washed with acetone. The residue was suspended in a little ethyl acetate and treated with saturated sodium bicarbonate solution. The organic phase was separated off, dried over magnesium sulfate, filtered and concentrated under reduced pressure. This synthesis yielded 2-(4-tert-butylphenoxymethyl)-6-chloro-8,8a-dihydroindeno [1,2-d]thiazol-3a-ol having a melting point of 122-124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06387935B1
Source datasetuspto-grants-2002_05
ORD IDord-89ecc1b48e754288b7f206b9123014bb
Source noteuspto-grants-2002_05