Octadecyl isocyanate → 4-n-Octadecylcarbamoyl-2,2,7,7-tetramethyl-1,4-diazacycloheptan-5-one

HRID 1657808Notes

Reaction equation

HRID 1657808 reaction equation
[CH3:1][C:2]1([CH3:12])[CH2:8][NH:7][C:6](=[O:9])[CH2:5][C:4]([CH3:11])([CH3:10])[NH:3]1.[CH2:13]([N:31]=[C:32]=[O:33])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30]>>[CH2:13]([NH:31][C:32]([N:7]1[C:6](=[O:9])[CH2:5][C:4]([CH3:11])([CH3:10])[NH:3][C:2]([CH3:12])([CH3:1])[CH2:8]1)=[O:33])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30]

Participants

3

Procedure

Using the same procedure as described in Example 4, 17 parts of 2,2,7,7-tetramethyl-1,4-diazacycloheptan-5-one and 32 parts of n-octadecyl isocyanate were reacted together and afforded 4-n-octadecylcarbamoyl-2,2,7,7-tetramethyl-1,4-diazacycloheptan-5-one as a colourless solid which was recrystallised from petroleum ether (of boiling range 60° to 80°C) and had a melting point of 56.5°-58°C. This material gave the following elemental analysis by weight:

Workup

  1. customwere reacted together

Sources & evidence

ORD record
ord-de2e28cf591c4d3594c23cdc28783396
Source dataset
uspto-grants-1976_06
Patent number
US03962255

Reaction notes

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