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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481615Generated: October 27, 2026

Methanol → (2S)-(-)-1-(4-indolyloxy)-3-(4-(2-methoxyphenyl)piperidin-1-yl)-2-propanol ethanedioate

https://huagongshe.com/reaction/481615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantOxalic AcidHCID 971—
Reactant4-(2-Methoxyphenyl)piperidineHCID 544738—
Reactant(2s)-Glycidyl indol-4-yl etherHCID 10943254—
SolventEthyl AcetateHCID 8857—
Product(2S)-(-)-1-(4-indolyloxy)-3-(4-(2-methoxyphenyl)piperidin-1-yl)-2-propanol ethanedioateHCID 131719700—

Reaction Steps

The title compound was prepared in similar fashion from (S)-(+)-4-(oxiranylmethoxy)-1H-indole and 4-(2-methoxyphenyl)piperidine. The resulting free base was dissolved in ethyl acetate, and precipitated with one equivalent of oxalic acid in ethyl acetate in 37% overall yield. FDMS m/e=380 (M+ of free base). α[D]589 =-14.83 (c=0.81, methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789402
Source datasetuspto-grants-1998_08
ORD IDord-546e4a5c72bc4d15a4788befb6445042
Source noteuspto-grants-1998_08