Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423170Generated: November 1, 2026

Acetyl chloride → 4-Bromo-1-(phenylsulfonyl)-1H-indol-5-yl acetate

https://huagongshe.com/reaction/2423170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant4-Bromo-1-(phenylsulfonyl)-1H-indol-5-olHCID 67242306—
SolventTetrahydrofuranHCID 8028—
Product4-Bromo-1-(phenylsulfonyl)-1H-indol-5-yl acetateHCID 6724133180.1%

Reaction Steps

Triethylamine (0.29 g, 2.8 mmol) was added to a solution of 4-bromo-1-(phenylsulfonyl)-1H-indol-5-ol (Intermediate 21, 0.67 g, 1.9 mmol) and acetyl chloride (0.22 g, 2.8 mmol) in THF (10 mL). The mixture was stirred for 10 minutes at room temperature and evaporated. The residue was partitioned between DCM and saturated aqueous NaHCO3. The reaction mixture was washed with saturated aqueous NaHCO3, and the organic phase was dried (MgSO4) and evaporated to give the title compound (0.6 g) as a red solid. MS m/z 394/396 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960374B2
Source datasetuspto-grants-2011_06
ORD IDord-ec6df60796c24876af7a0efac1d59ebd
Source noteuspto-grants-2011_06