Triethanolamine → HCID 10344883, compound

HRID 420430Notes

Reaction equation

HRID 420430 reaction equation
[CH2:1]([O:13][S:14]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)(=[O:16])=[O:15])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[N:23]([CH2:30][CH2:31][OH:32])([CH2:27][CH2:28][OH:29])[CH2:24][CH2:25][OH:26]>>[N:23]([CH2:30][CH2:31][OH:32])([CH2:27][CH2:28][OH:29])[CH2:24][CH2:25][OH:26].[CH2:1]([O:13][S:14]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)(=[O:16])=[O:15])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]

Participants

3

Reactant 2

HCID 7618TriethanolamineHCID 15900Dodecyl benzenesulfonate

Product 1

HCID 10344883HCID 10344883, compound

Procedure

1200 g of linear dodecylbenzenesulfonate was heated (50 to 60° C.) while being stirred. Triethanolamine was added dropwise while keeping the temperature constant (50 to 60° C.) until the pH of the system increased to approximately 6 to obtain a linear dodecylbenzenesulfonate triethanolamine salt.

Workup

  1. customthe temperature constant (50 to 60° C.)
  2. temperatureincreased to approximately 6

Sources & evidence

ORD record
ord-3e547d02242147079d587b916df0cc26
Source dataset
uspto-grants-2012_01
Patent number
US08097563B2

Reaction notes

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