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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719116Generated: October 31, 2026

Water → 5-Benzyloxy-2-(4-benzyloxy-phenyl)-1-[4-(3-chloro-propoxy)-benzyl]-3-methyl-1H-indole

https://huagongshe.com/reaction/719116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1H-Indole, 3-methyl-5-(phenylmethoxy)-2-[4-(phenylmethoxy)phenyl]-HCID 3824745—
Reactant4-(3-Chloropropoxy)-benzyl bromideHCID 21882276—
SolventDimethylformamideHCID 6228—
Product5-Benzyloxy-2-(4-benzyloxy-phenyl)-1-[4-(3-chloro-propoxy)-benzyl]-3-methyl-1H-indoleHCID 12133138—

Reaction Steps

A solution consisting of 5-Benzyloxy-2-(4-benzyloxy-phenyl)-3-methyl-1H-indole No. 7 (6.5 g, 15.5 mmol) in DMF (60 mL) was cooled to 0° C. and treated with addition of sodium hydride (0.68 g, 17.0 mmol) and stirred for 20 minutes. A solution of 4-(3-chloropropoxy)-benzyl bromide No. 163 in DMF (10 mL) was then added slowly. The reaction was allowed to come to rt and stirred for 2 hours. The reaction was poured into water and extracted with ethyl acetate. The ethyl acetate was washed with water, brine and dried over magnesium sulfate and concentrated. The concentrate was treated with methanol and 5 g of the desired product precipitated as a white solid with a melting point of 130–132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132417B2
Source datasetuspto-grants-2006_11
ORD IDord-25757f9aaec346b5b6be776a758c5a8f
Source noteuspto-grants-2006_11