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Thionyl Chloride → 4-(Chloromethyl)-4'-(octyloxy)-1,1'-biphenyl

HRID 2231802
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HRID 2231802 반응식
[CH2:1]([O:9][C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:21]=[CH:20][C:19]([CH2:22]O)=[CH:18][CH:17]=2)=[CH:12][CH:11]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].S(Cl)([Cl:26])=O>C1(C)C=CC=CC=1>[CH2:1]([O:9][C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:21]=[CH:20][C:19]([CH2:22][Cl:26])=[CH:18][CH:17]=2)=[CH:12][CH:11]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 13878907HCID 13878907, 화합물

생성물 1

HCID 137419724-(Chloromethyl)-4'-(octyloxy)-1,1'-biphenyl

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
70 °C

실험 절차

A mixture of 30 g of 4'-octyloxy-4-formylbiphenyl, 2.0 g of sodium borohydride and 300 ml of isopropanol was stirred on a water bath maintained at 70° C. for 3 hours. 20 ml of 6 N hydrochloric acid and 10 ml of water were added, and the resulting mixture was stirred for 2 hours. The reaction mixture was allowed to cool and filtered to collect solids. These solids were recrystallized from 300 ml of ethanol to obtain 30 g of 4'-octyloxy-4-hydroxymethyl-biphenyl. The total of 4'-octyloxy-4-hydroxymethyl-biphenyl, 100 ml of toluene and 40 g of thionyl chloride were uniformly mixed and allowed to stand overnight at room temperature. Then, the mixture was heated for 30 minutes on a water bath maintained at 70° C. After being allowed to cool, the mixture was poured into ice water and then extracted with 300 ml of toluene. The extract was washed with saturated saline water, with a saturated aqueous sodium hydrogen-carbonate and further with saturated saline water to make it neutral. Then, the extract was dried over anhydrous magnesium sulfate, concentrated and then recrystallized from 300 ml of ethanol to obtain 26 g of 4'-octyloxy-4-chloromethyl-biphenyl having a melting point of 97.3 to 98.0° C. Analysis of the compound by HPLC showed that the purity was 99.6%. (ii) Preparation of Objective Compound

후처리

  1. temperatureThen, the mixture was heated for 30 minutes on a water bath
  2. temperatureto cool
  3. extractionextracted with 300 ml of toluene
  4. washThe extract was washed with saturated saline water, with a saturated aqueous sodium hydrogen-carbonate and further with saturated saline water
  5. dry with materialThen, the extract was dried over anhydrous magnesium sulfate
  6. concentrationconcentrated
  7. customrecrystallized from 300 ml of ethanol

출처 및 근거

ORD 기록
ord-459bb0c95abf422fafefa2eb6c07048a
출처 데이터셋
uspto-grants-1988_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04784791

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