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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11748Generated: October 26, 2026

Phosphorus tribromide → tert-butyl 4-(bromomethyl)-1H-indole-1-carboxylate

https://huagongshe.com/reaction/11748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus tribromideHCID 24614—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl 4-(hydroxymethyl)-1H-indole-1-carboxylateHCID 12148524—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Producttert-butyl 4-(bromomethyl)-1H-indole-1-carboxylateHCID 1214852584%

Reaction Steps

PBr3 (2.4 mL. 25.8 mmol) was added dropwise at 0° C. under nitrogen to a stirred solution of tert-butyl 4-(hydroxymethyl) 1H-1-indolecarboxylate 6 (6.0 g, 24.3 mmol) in ether (80 mL) and CH2Cl2 (20 mL) under nitrogen. The reaction was completed 30 minutes after the addition. The mixture was poured into a cold aqueous NaHCO3 solution (100 mL) and extracted with ethyl acetate (3×80 mL). The combined extract was washed sequentially with water (80 mL), and brine (80 mL), then dried (MgSO4), filtered, and finally concentrated to provide tert-butyl 4-(bromomethyl)-1H-1-indolecarboxylate 7 (6.3 g, 84%) as an oil which was immediately taken to the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098307B2
Source datasetuspto-grants-2006_08
ORD IDord-5f42e2530e154a3096b9b9ddf20e8732
Source noteuspto-grants-2006_08