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1-Dodecanol → HCID 20363224, 화합물

HRID 918243
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HRID 918243 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][CH:10]([CH:5]([S:1]([OH:4])(=[O:3])=[O:2])[C:6]([O-:25])=[O:7])[C:9]([O-:8])=[O:11])[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 20363224HCID 20363224, 화합물수율 64.2%

시약·촉매·용매 1

HCID 962Water용매

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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-c9ee13e408c7468f8cf1a12dfef201bd
출처 데이터셋
uspto-grants-1976_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03970653

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