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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602491Generated: October 25, 2026

2-Bromocyclohexanone → Methyl 3-(4,5,6,7-tetrahydrobenzothiazol-2-ylmethoxy)benzoate

https://huagongshe.com/reaction/1602491

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromocyclohexanoneHCID 11789758—
ReactantMethyl 3-thiocarbamoylmethoxybenzoateHCID 19611422—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 3-(4,5,6,7-tetrahydrobenzothiazol-2-ylmethoxy)benzoateHCID 1961152127.3%

Reaction Steps

After a mixture of 2-bromocyclohexanone (865 mg, 4.9 mmol), methyl 3-(thiocarbamoylmethoxy)benzoate (1.00 g, 4.4 mmol) and 1,4-dioxane (10 ml) was stirred at room temperature for 5 hours and then at 80° C. for 12 hours, it was cooled and concentrated under reduced pressure. Saturated sodium bicarbonate aqueous solution was added to the resulting residue and the product formed was extracted with ethyl acetate. The extract was washed with water and brine in that order, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. Thereafter, the resulting residue was purified by silica gel column chromatography (eluent=hexane:ethyl acetate=4:1) to give methyl 3-(4,5,6,7-tetrahydrobenzothiazol-2-ylmethoxy)benzoate (369 mg, 1.2 mmol, 27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981559
Source datasetuspto-grants-1999_11
ORD IDord-90d3decdfeb643aebe6f0ba671ed51e1
Source noteuspto-grants-1999_11