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1-Dodecanol → HCID 21523798, 화합물

HRID 917834
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HRID 917834 반응식
[S:1]([C:5]1[C:6]([O:8][C:9](=[O:11])[CH:10]=1)=[O:7])([OH:4])(=[O:3])=[O:2].[CH2:12]([OH:24])[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23].[OH-:25].[Na+:26]>O>[CH2:12]([O:24][C:5]([S:1]([OH:4])(=[O:3])=[O:2])([CH2:10][C:9]([O-:8])=[O:11])[C:6]([O-:25])=[O:7])[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23].[Na+:26].[Na+:26].[Na+:26]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 81931-DodecanolHCID 14798Sodium HydroxideHCID 12479880Sulfomaleic anhydride

생성물 1

HCID 21523798HCID 21523798, 화합물수율 64.2%

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
100 °C

실험 절차

Sulfomaleic anhydride (10 gm) is mixed with 80 gm (0.45 mole) of n-dodecanol and heated at 100°C for 14 hours. A solution of 7.04 gm of sodium hydroxide in 50 ml water is then added and the mixture heated at 60°C for 2 hours. The heated mixture is then extracted three times with 300 cc portions of acetone (at reflux) and the acetone insoluble fraction is then filtered, washed with additional acetone and dried to give 16.2 gm of the title compound (structure confirmed by NMR and ion exchange of a sample followed by titration with standard sodium hydroxide: neutralization equivalent: found 147.0, theory 149.3).

후처리

  1. temperaturethe mixture heated at 60°C for 2 hours
  2. extractionThe heated mixture is then extracted three times with 300 cc portions of acetone (at reflux)
  3. filtrationthe acetone insoluble fraction is then filtered
  4. washwashed with additional acetone
  5. customdried

출처 및 근거

ORD 기록
ord-83e831bae99d4793bdc03596dd3df19f
출처 데이터셋
uspto-grants-1976_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03968110

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