2,2-Dimethylbutyryl chloride → HCID 21804161, compound

HRID 1757328Notes

Reaction equation

HRID 1757328 reaction equation
[O:1]1[CH2:21][CH2:20][O:19][CH2:18][CH2:17][NH:16][CH2:15][CH2:14][O:13][CH2:12][CH2:11][O:10][CH2:9][CH2:8][O:7][CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[CH3:22][C:23]([CH3:29])([CH2:27][CH3:28])[C:24](Cl)=[O:25]>>[CH3:22][C:23]([CH3:29])([CH2:27][CH3:28])[C:24]([N:4]1[CH2:5][CH2:6][O:7][CH2:8][CH2:9][O:10][CH2:11][CH2:12][O:13][CH2:14][CH2:15][N:16]([C:24](=[O:25])[C:23]([CH3:29])([CH3:22])[CH2:27][CH3:28])[CH2:17][CH2:18][O:19][CH2:20][CH2:21][O:1][CH2:2][CH2:3]1)=[O:25]

Participants

3

Reactant 2

HCID 799582,2-Dimethylbutyryl chlorideHCID 903221,4,7,13,16-Pentaoxa-10,19-diazacyclohenicosane

Product 1

HCID 21804161HCID 21804161, compound

Procedure

Analogously to Example 2 from 1,7,10,13,19-pentaoxa-4,16-diazacycloheneicosane and 2,2-dimethylbutyryl chloride. Example 30

Sources & evidence

ORD record
ord-8d7c8d8c02da4f0ba60c276c684e482e
Source dataset
uspto-grants-1995_08
Patent number
US05445762

Reaction notes

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