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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355868Generated: October 25, 2026

tert-Butoxy bis(dimethylamino)methane → 4-[(dimethylamino)methylene]-1,2,3,4-tetrahydro-1-(4-nitrobenzoyl)-5H-1-benzazepin-5-one

https://huagongshe.com/reaction/355868

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butoxy bis(dimethylamino)methaneHCID 79885—
Reactant5H-1-Benzazepin-5-one, 1,2,3,4-tetrahydro-1-(4-nitrobenzoyl)-HCID 10733729—
Product4-[(dimethylamino)methylene]-1,2,3,4-tetrahydro-1-(4-nitrobenzoyl)-5H-1-benzazepin-5-oneHCID 53653564—

Reaction Steps

A mixture of 1.35 g of 1,2,3,4-tetrahydro-1-(4-nitrobenzoyl)-5H-1-benzazepin-5-one and 15 ml of tert-butoxy-bis(dimethylamino)methane is heated for on a steam bath for 2 hours. The volatiles are evaporated in vacuo to a residue which is stirred with ether and filtered. The cake is washed with ether and the combined filtrates evaporated in vacuo to a residue which is dissolved in 30% ethyl acetate in methylene chloride and passed through a pad of hydrous magnesium silicate. The filtrate is evaporated in vacuo to a residue which is dissolved in 30% ethyl acetate in methylene chloride and passed through a pad of hydrous magnesium silicate. The filtrate is evaporated in vacuo to a residue to give 1.60 g of yellow crystalline product, m.p. 180°-183° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834461
Source datasetuspto-grants-1998_11
ORD IDord-6530b21b14864ff38f3f266efa748f7a
Source noteuspto-grants-1998_11