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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369769Generated: October 25, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 23282674, compound

https://huagongshe.com/reaction/369769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant1-Benzyl-4-piperidoneHCID 19220—
Reactant2,3-Dihydro-2,2-dimethylbenzofuranHCID 80640—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
SolventHeptaneHCID 8900—
ProductHCID 23282674HCID 2328267419.3%

Reaction Conditions

Temperature35 °C

Reaction Steps

A mixture of 2,3-dihydro-2,2-dimethylbenzofuran (25 g) and tetramethylethylenediamine (46 g) in heptane (250 ml) was treated dropwise at room temperature with 1.6 M BuLi in hexane (250 ml). After stirring for 1.5 h at 30-40° C. the mixture was cooled to -40° C. and 1-benzyl-4-piperidinone (32 g) was added dropwise at -40° C. The reaction mixture was allowed to warm to room temperature during 3 h followed by quench with water. After concentrating the reaction mixture in vacuo dichloromethane (500 ml) was added followed by wash with water (3×500 ml). Removal of solvent in vacuo gave an oil which was purified by flash chromatography (silica gel, heptane/ethyl acetate/triethylamine 50:48:2) giving an oil. Addition of heptane gave the product, 7-(1-benzyl-4-hydroxy-4-piperidinyl)-2,3-dihydro-2,2-dimethylbenzofuran as a solid (11 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140331
Source datasetuspto-grants-2000_10
ORD IDord-473a973c775e47bfa3c6acd82b096acc
Source noteuspto-grants-2000_10