Palmitoyl chloride → HCID 19735235, compound

HRID 326542Notes

Reaction equation

HRID 326542 reaction equation
[CH3:1][N:2]([CH3:9])[CH2:3][CH2:4][CH2:5][NH:6][CH2:7][CH3:8].[C:10](Cl)(=[O:26])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]>C(Cl)Cl>[CH3:1][N:2]([CH3:9])[CH2:3][CH2:4][CH2:5][N:6]([CH2:7][CH3:8])[C:10](=[O:26])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]

Participants

4

Reactant 2

HCID 8206Palmitoyl chlorideHCID 88082N'-Ethyl-N,N-dimethylpropane-1,3-diamine

Product 1

HCID 19735235HCID 19735235, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of N,N-dimethyl-N'-ethyl-1,3-propanediamine (1.18 g, 9.06 mmole) in methylene chloride (20 mL) was added palmitoyl chloride (2.20 g, 8.00 mmole) dropwise. The reaction mixture was stirred at room temperature overnight.

Sources & evidence

ORD record
ord-a4e0c002d15a4ce1844a89a0b2bff17a
Source dataset
uspto-grants-1993_12
Patent number
US05270310

Reaction notes

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