Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377984Generated: November 1, 2026

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

https://huagongshe.com/reaction/2377984

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 numberUS07470710B2
Source datasetuspto-grants-2008_12
ORD IDord-60f05cf6c9384b0893b3da2dc835b776
Source noteuspto-grants-2008_12