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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069653Generated: October 29, 2026

N-bromobutanimide → HCID 54103301, compound

https://huagongshe.com/reaction/1069653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 10805854HCID 10805854—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 54103301HCID 5410330143%

Reaction Steps

A mixture of 5-methoxy-1-(phenylmethyl)-1H-indole-3-acetic acid ethyl ester (10.8 g, 32 mmol) and 6.3 g (35 mmol) of N-bromosuccinimide in 250 mL of carbon tetrachloride was stirred for 1.5 hours, washed with Na2S2O3 solution, water, brine, and dried (Na2SO4). After concentrating at reduced pressure, the residue was chromatographed on silica gel and eluted with a gradient, 25% ether/hexane→40% ether/hexane, to give 5.5 g (43% yield) of 2-bromo-5-methoxy-1-(phenylmethyl)-1H-indole-3-acetic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06252084B1
Source datasetuspto-grants-2001_06
ORD IDord-536d23711a8d47eaab6ccf3b30f6fc29
Source noteuspto-grants-2001_06