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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484254Generated: October 25, 2026

p-Toluenesulfonic acid → 1,3,4,9-Tetrahydro-1,1-diethyl-6-(phenylmethoxy)pyrano[3,4-b]indole

https://huagongshe.com/reaction/484254

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantEthyl ketoneHCID 7288—
Reactant5-Benzyloxy-3-(2-hydroxyethyl)indoleHCID 744849—
SolventBenzeneHCID 241—
Product1,3,4,9-Tetrahydro-1,1-diethyl-6-(phenylmethoxy)pyrano[3,4-b]indoleHCID 19935702—

Reaction Steps

A mixture consisting of 5-benzyloxytryptophol (7.0 g, 0.0262 mol), diethyl ketone (10 mL), benzene (400 mL) and p-toluene sulfonic acid is refluxed for 3.5 hours using a Dean-Stark tap to remove the water. The reaction mixture is cooled to room temperature, washed with 5% sodium bicarbonate, water (200 mL), brine (200 mL), dried (MgSO4), filtered and concentrated to give 9.9 g of crude product. The crude product is flash chromatographed on silica gel using 15% ethyl acetate/hexane as an eluent to afford 6.5 g of pure title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05229516
Source datasetuspto-grants-1993_07
ORD IDord-88eb7c4714a24a96b46031d2ea298e13
Source noteuspto-grants-1993_07