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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371865Generated: October 31, 2026

Sodium borohydride → 7-chloro-1H-indole

https://huagongshe.com/reaction/1371865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(2-Amino-3-chlorophenyl)-2-chloroethan-1-oneHCID 12477778—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product7-chloro-1H-indoleHCID 104644—

Reaction Steps

Dissolve 1-(2-amino-3-chlorophenyl)-2-chloroethanone (7.0 g, 34.30 mmol) in 10% aqueous 1,4-dioxane (75 mL). Carefully add NaBH4 (2.6 g, 68.6 mmol, 2 eq.) as a solid. Heat to reflux. After 4 hours, cool to room temperature, dilute with water (300 mL), and extract with dichloromethane (2×200 mL). Combine the organic layers, dry over MgSO4, filter, and remove the solvent in vacuo leaving a light brown oil in the flask. Purify the oil by HPLC (silica gel mobile phase: 100% hexane to 50% EtOAc in hexanes over 50 minutes), to give the title compound as a brown oil: 1H NMR (300 MHz, d6-DMSO-d6): 5.16 (m, 1H), 5.39 (d, 1H), 5.70 (bs, 1H), 6.59 (t, 1H), 7.09 (m, 2H); MS (ES+): m/z 154, 152 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157488B2
Source datasetuspto-grants-2007_01
ORD IDord-5f4262191c1c49d4b059d8c283e33bd9
Source noteuspto-grants-2007_01