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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493197Generated: November 1, 2026

Triphenylphosphine → 4-(2-Ethoxycarbonyl-benzo[b]thiophen-6-yloxy)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/493197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantEthyl 6-hydroxybenzo[b]thiophene-2-carboxylateHCID 58047243—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Ethoxycarbonyl-benzo[b]thiophen-6-yloxy)-piperidine-1-carboxylic acid tert-butyl esterHCID 6872658194.4%

Reaction Steps

The above prepared 6-hydroxy-benzo[b]thiophene-2-carboxylic acid ethyl ester (0.206 g, 0.927 mmol, see example 7, step 1 and 2) was dissolved in 5 mL of THF and treated successively at −10° C. with 4-hydroxy-piperidine-1-carboxylic acid tert-butyl ester (0.261 g, 1.4 eq.), triphenylphosphine (0.340 g, 1.4 eq.) and DIAD (0.255 mL, 2 eq.), and the mixture then kept at ambient temperature over night. Pouring onto crashed ice, twofold extraction with AcOEt, washing with water and brine, drying over magnesium sulfate, and evaporation of the solvents, followed by flash chromatography (SiO2, hexane AcOEt=85/15), yielded 0.355 g of the title compound as colorless gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534788B2
Source datasetuspto-grants-2009_05
ORD IDord-f4fc7e9fcad54b32879d46e56b223619
Source noteuspto-grants-2009_05