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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821936Generated: November 1, 2026

Boc-indole → tert-Butyl-1-[2-acetoxy-3-(4-octylphenoxy)propyl]indole-2-carboxylate

https://huagongshe.com/reaction/1821936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoc-indoleHCID 11458614—
ReactantHCID 86606004HCID 86606004—
SolventDimethyl SulfoxideHCID 679—
SolventSodium ChlorideHCID 5234—
Producttert-Butyl-1-[2-acetoxy-3-(4-octylphenoxy)propyl]indole-2-carboxylateHCID 11526497—

Reaction Conditions

Temperature110 °C

Reaction Steps

0.325 g (1.50 mmol) tert-butylindole-2-carboxylate is dissolved in 15 ml absolute DMSO, mixed with 0.184 g (1.64 mmol) potassium-tert-butylate and stirred at 110° C. for 15 min. A solution of 0.576 g (1.50 mmol) [1-bromo-3-(4-octylphenoxy)propan-2-yl]acetate in 15 ml absolute DMSO is added drop-wise. Following 30 minutes of heating at 110° C. and subsequent cooling, hydrolysis is carried out in saturated NaCl solution. Four extractions with diethyl ether, combination of the organic phases, concentration to half the volume on the rotary evaporator, three wash steps with saturated NaCl solution, drying on sodium sulfate, filtration and reconcentration on the rotary evaporator leave as a crude product a yellow oil which is purified on silica gel by means of flash column chromatography (flow agent: petroleum ether/ethyl acetate 99:1) and yields the product as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608633B2
Source datasetuspto-grants-2009_10
ORD IDord-5f644bd9e7ff4654953bc9d2d697a932
Source noteuspto-grants-2009_10