Butyl chloroformate → HCID 19385950, compound
Reaction equation
[C:1](Cl)(=[O:7])[O:2][CH2:3][CH2:4][CH2:5][CH3:6].[CH3:9][C:10]1([CH3:32])[CH2:15][CH:14]([NH:16][CH2:17][CH2:18][NH:19][CH:20]2[CH2:25][C:24]([CH3:27])([CH3:26])[NH:23][C:22]([CH3:29])([CH3:28])[CH2:21]2)[CH2:13][C:12]([CH3:31])([CH3:30])[NH:11]1>O>[CH2:3]([O:2][C:1]([N:16]([CH:14]1[CH2:15][C:10]([CH3:32])([CH3:9])[NH:11][C:12]([CH3:31])([CH3:30])[CH2:13]1)[CH2:17][CH2:18][N:19]([C:1]([O:2][CH2:3][CH2:4][CH2:5][CH3:6])=[O:7])[CH:20]1[CH2:21][C:22]([CH3:29])([CH3:28])[NH:23][C:24]([CH3:27])([CH3:26])[CH2:25]1)=[O:7])[CH2:4][CH2:5][CH3:6]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
120.2 g (0.88 mol) of butyl chlorocarbonate are reacted as described in Example 1 with 135.4 g (0.4 mol) of N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,2-ethanediamine dissolved in 410 ml of water.
Sources & evidence
- ORD record
- ord-fa2be408ecab4b449fcaaf48d47dac5a
- Source dataset
- uspto-grants-1995_09
- Patent number
- US05449779
Reaction notes
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