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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829115Generated: November 1, 2026

Acetic Acid → TERT-BUTYL 4-(INDOLIN-1-YL)PIPERIDINE-1-CARBOXYLATE

https://huagongshe.com/reaction/1829115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantIndolineHCID 10328—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
ProductTERT-BUTYL 4-(INDOLIN-1-YL)PIPERIDINE-1-CARBOXYLATEHCID 1144951374.3%

Reaction Steps

1-tert-Butoxycarbonylpiperidin-4-one (2.50 g), indoline (1.50 g) and acetic acid (0.73 mL) were dissolved in 1,2-dichloroethane (75 mL), and sodium triacetoxyborohydride (5.32 g) was added thereto. The mixture was stirred at room temperature for 12 hr. The reaction mixture was added to iced water and the mixture was extracted with chloroform. The extract was dried and the solvent was evaporated under reduced pressure. The residue was purified by silica gel chromatography to give 1-tert-butoxycarbonyl-4-(1-indolinyl)piperidine (2.82 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060722B2
Source datasetuspto-grants-2006_06
ORD IDord-9623dd8a86dd4cb0a3fc666760c7d92c
Source noteuspto-grants-2006_06