Dimethylamine → HCID 20536210, compound

HRID 1155967Notes

Reaction equation

HRID 1155967 reaction equation
[C:1]([C:3]1[CH:4]=[CH:5][C:6]2[O:10][C:9](=[O:11])[C:8]([CH3:13])([CH3:12])[C:7]=2[CH:14]=1)#[N:2].[CH3:15][NH:16][CH3:17]>C(OCC)C.C(O)C>[OH:10][C:6]1[CH:5]=[CH:4][C:3]([C:1]#[N:2])=[CH:14][C:7]=1[C:8]([CH3:13])([CH3:12])[C:9]([N:16]([CH3:17])[CH3:15])=[O:11]

Participants

5

Reactant 2

HCID 674DimethylamineHCID 205362475-Cyano-2,3-dihydro-3,3-dimethylbenzofuran-2-one

Product 1

HCID 20536210HCID 20536210, compound

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 3283Diethyl EtherSolvent

Procedure

A suspension of 5-cyano-2,3-dihydro-3,3-dimethylbenzofuran-2-one (3.7 g), prepared as in Example 3, in diethyl ether (50 ml) was treated with a solution of dimethylamine in ethanol (8.6 ml of a 20.8% solution) portionwise with stirring at room temperature. The mixture was stirred for two hours, and the product was isolated by filtration, yield 4 g, mp 146°-148° C.

Workup

  1. stirringThe mixture was stirred for two hours
  2. customthe product was isolated by filtration, yield 4 g, mp 146°-148° C.

Sources & evidence

ORD record
ord-d588f7db16ca47c191e3916c03866eb8
Source dataset
uspto-grants-1982_06
Patent number
US04333759

Reaction notes

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