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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Reactant | 2,3-Dihydro-2,2-dimethylbenzofuran | HCID 80640 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | HCID 23282674 | HCID 23282674 | 19.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06140331 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-473a973c775e47bfa3c6acd82b096acc |
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| Source note | uspto-grants-2000_10 |
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