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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989165Generated: October 30, 2026

Bromine → Thiocyanic acid, 2,3-dihydro-6-(trifluoromethyl)-1H-indol-5-yl ester

https://huagongshe.com/reaction/989165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantPotassium thiocyanateHCID 516872—
Reactant6-(Trifluoromethyl)indolineHCID 10176437—
SolventMethanolHCID 887—
ProductThiocyanic acid, 2,3-dihydro-6-(trifluoromethyl)-1H-indol-5-yl esterHCID 1061028372%

Reaction Steps

A mixture of trifluoromethylindoline (D1) (9.7 g, 52 mmol) and potassium thiocyanate (10.09 g, 104 mmol) in methanol (200 ml) was treated with a solution of bromine (2.82 ml, 55 mmol) in methanol (35 ml) dropwise over 0.5 h at −5-0° C. The reaction mixture was allowed to warm to room temperature and stirred overnight then evaporated to dryness. The residue was partitioned between aqueous K2CO3 (100 ml) and dichloromethane (3×100 ml). The combined extracts were dried (Na2SO4) and evaporated and the residue chromatographed on silica using 2-30% ethyl acetate/petroleum ether as eluant to afford the title compound (9.1 g, 72%) as a yellow solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638953B2
Source datasetuspto-grants-2003_10
ORD IDord-5442307bae824ea9aae7985800a7252d
Source noteuspto-grants-2003_10