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1,2-Dibromoethane → HCID 18362251, 화합물

HRID 382908
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HRID 382908 반응식
[CH2:1]([O:4][C:5]1[CH:6]=[C:7]([OH:11])[CH:8]=[CH:9][CH:10]=1)[CH2:2][CH3:3].[Br:12][CH2:13][CH2:14]Br.[OH-].[Na+]>S([O-])(O)(=O)=O.C([N+](CCCC)(CCCC)CCCC)CCC.O>[Br:12][CH2:13][CH2:14][O:11][C:7]1[CH:8]=[CH:9][CH:10]=[C:5]([O:4][CH2:1][CH2:2][CH3:3])[CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 78391,2-DibromoethaneHCID 14798Sodium Hydroxide2회HCID 111162393-propoxyphenol

생성물 1

HCID 18362251HCID 18362251, 화합물수율 97%

시약·촉매·용매 2

HCID 94433Tetrabutylammonium hydrogen sulfate촉매HCID 962Water용매2회

실험 절차

A solution of 3-(n-propoxy)phenol (15.2 g; 0.1 mol; from Example A above) in 1,2-dibromoethane (100 ml; 1.16 mol) was added to a solution of tetrabutylammonium hydrogen sulphate (34 g; 0.1 mol) and sodium hydroxide (8.0 g; 0.2 mol) in water (100 ml). The mixture was stirred vigorously whilst a 50% solution of sodium hydroxide in water (33 ml) was added dropwise over half an hour. Stirring was subsequently continued for one hour. The organic phase was separated, washed with water and dried over magnesium sulphate. The solvent was evaporated and the residue treated with diethyl ether (150 ml). The precipitated salt was removed by filtration and the diethyl ether evaporated. The residue was distilled to yield (14.0 g; 54%) of the title compound as an oil (97% purity). bp 112-115° C. (0.05 mm Hg) MW=259 (GC-MS)

후처리

  1. additionwas added dropwise over half an hour
  2. customThe organic phase was separated
  3. washwashed with water
  4. dry with materialdried over magnesium sulphate
  5. customThe solvent was evaporated
  6. additionthe residue treated with diethyl ether (150 ml)
  7. customThe precipitated salt was removed by filtration
  8. customthe diethyl ether evaporated
  9. distillationThe residue was distilled

출처 및 근거

ORD 기록
ord-b4e2c18fbc384a2994ade43314599ec0
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06310252B1

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