Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077276Generated: November 3, 2026

(RS)-2-(2-Benzofuranylcarbonyl)-1-(tert-butyloxycarbonyl)piperidine → HCID 23146318, compound

https://huagongshe.com/reaction/2077276

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(RS)-2-(2-Benzofuranylcarbonyl)-1-(tert-butyloxycarbonyl)piperidineHCID 23146395—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 23146318HCID 2314631899%

Reaction Steps

A solution of (RS)-2-(2-benzofuranylcarbonyl)-1-(tert-butyloxycarbonyl)piperidine, D2 (0.86 g, 2.61 mmol) in trifluoroacetic acid (5 ml) and dichloromethane (20 ml) was warmed at 35° C. for 0.5 h. The reaction mixture was evaporated in vacuo and the residue partitioned between dichloromethane (30 ml) and 1N sodium hydroxide (30 ml). The aqueous layer was extracted with dichloromethane (30 ml) and the combined organic layers dried (Na2SO4) and evaporated in vacuo to afford the title compound as a pale yellow gum (0.59 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928124B2
Source datasetuspto-grants-2011_04
ORD IDord-1e31b1364b58480dbcaaec13d3e82f4f
Source noteuspto-grants-2011_04