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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366977Generated: October 27, 2026

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

https://huagongshe.com/reaction/1366977

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 numberUS07893090B2
Source datasetuspto-grants-2011_02
ORD IDord-d4d6a322665a4ed9a22fbe1f9cefb67c
Source noteuspto-grants-2011_02