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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Veratryl alcohol → Veratryl chloride

HRID 339649
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HRID 339649 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[CH2:6]O.S(Cl)([Cl:15])=O>C1(C)C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[CH2:6][Cl:15]
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참가 물질

4

반응물 2

HCID 7118Veratryl alcoholHCID 24386Thionyl Chloride

생성물 1

HCID 81740Veratryl chloride

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
0 °C

실험 절차

3,4-dimethoxybenzyl alcohol (20 g, 119 mmol) was dissolved in toluene (60 ml) and cooled to 0° C. Thionyl chloride (7.48 g, 61.4 mmol) was added dropwise to the cooled solution of the alcohol over a period of 30 minutes, and the reaction was maintained at 0° C. for an additional 30 minutes. The reaction was quenched by pouring onto an ice/water mix (100 ml), and the organic phase was separated. The aqueous phase was then extracted into toluene (2×20 ml) and the combined toluene solution was dried over anhydrous sodium sulfate. The toluene was removed at reduced pressure to afford an oil which solidified upon standing, with a yield of 21 g. The material was characterized as a single spot by thin layer chromatography (TLC).

후처리

  1. temperaturethe reaction was maintained at 0° C. for an additional 30 minutes
  2. customThe reaction was quenched
  3. additionby pouring onto an ice/water
  4. additionmix (100 ml)
  5. customthe organic phase was separated
  6. extractionThe aqueous phase was then extracted into toluene (2×20 ml)
  7. dry with materialthe combined toluene solution was dried over anhydrous sodium sulfate
  8. customThe toluene was removed at reduced pressure
  9. customto afford an oil which

출처 및 근거

ORD 기록
ord-182dff26fd8a47de90ddcafc14b88847
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895554B2

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