Potassium Hydroxide → HCID 86755848, compound
Reaction equation
[OH-].[K+:2].[C:3]([CH2:5][CH2:6][N:7]([C:12](=[O:24])[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])[CH2:8][C:9]([OH:11])=[O:10])#[N:4]>>[C:3]([CH2:5][CH2:6][N:7]([C:12](=[O:24])[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])[CH2:8][C:9]([O-:11])=[O:10])#[N:4].[K+:2]Participants
3
Procedure
A 30% aqueous solution of KOH was gradually added to the N-cyanoethyl-N-dodecanoylglycine obtained in Example 2 to thereby adjust the pH of the system to 6.0. Thus, an aqueous solution of potassium N-cyanoethyl-N-dodecanoylglycinate was obtained. 1H-NMR spectrum (200 MHz, D2O) 4.02 (s,1 H), 3.94 (s,1 H), 3.76 (t,1 H), 3.65 (t,1 H), 2.80 (t,1 H), 2.71 (t,1 H), 2.50 (t,1 H), 2.30 (t,1 H), 1.60 (m,2 H), 1.31 (b,16 H), 0.89 (t,3 H) ppm
Sources & evidence
- ORD record
- ord-26f8a25c7cb6440787517c022ee6fb38
- Source dataset
- uspto-grants-2000_09
- Patent number
- US06121470
Reaction notes
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