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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetyl chloride → Methyl 2-(3-acetyl-4-hydroxyphenyl)propionate

HRID 26680
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HRID 26680 반응식
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]([CH3:14])[C:10]([O:12][CH3:13])=[O:11])=[CH:5][CH:4]=1.[C:15](Cl)(=[O:17])[CH3:16].B(Cl)(Cl)Cl>ClCCl.[Ti](Cl)(Cl)(Cl)Cl>[C:15]([C:4]1[CH:5]=[C:6]([CH:9]([CH3:14])[C:10]([O:12][CH3:13])=[O:11])[CH:7]=[CH:8][C:3]=1[OH:2])(=[O:17])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 6367Acetyl chlorideHCID 25135Boron TrichlorideHCID 12398855Methyl 2-(4-methoxyphenyl)propanoate

생성물 1

HCID 21322000Methyl 2-(3-acetyl-4-hydroxyphenyl)propionate

시약·촉매·용매 2

HCID 24193Titanium Tetrachloride촉매HCID 6344Dichloromethane용매

실험 절차

Titanium tetrachloride (82.3 mls) was added dropwise to a stirred solution of methyl 2-(4-methoxyphenyl)propionate (25 g) in dry dichloromethane (250 mls), cooled in an ice/salt-bath, at a rate sufficient to maintain the temperature between -10° C. and -5° C. The mixture was stirred for 10 minutes and acetyl chloride (10 g) was added dropwise at a rate sufficient to maintain the temperature below 0° C. The solution was stirred at -5° C. for 11/2 hours when boron trichloride (15 mls) was added. Stirring was continued for 1/2 hour at +3° C. before pouring on to crushed ice/concentrated hydrochloric acid and separating the two phases. The aqueous phase was extracted with ether (3x) and the combined organic extracts were washed with saturated sodium bicarbonate solution, saturated brine solution, and dried over anhydrous magnesium sulphate. Evaporation of the solvent yielded the crude product as a pale yellow oil. Vacuum distillation furnished a pale yellow oil bp 120°-125° C./0.15 mm (16.2 g; 59%)

후처리

  1. temperaturecooled in an ice/salt-bath, at a rate sufficient
  2. temperatureto maintain the temperature between -10° C. and -5° C
  3. temperatureto maintain the temperature below 0° C
  4. additionwas added
  5. stirringStirring
  6. waitwas continued for 1/2 hour at +3° C.
  7. additionbefore pouring on
  8. customto crushed ice/concentrated hydrochloric acid
  9. customseparating the two phases
  10. extractionThe aqueous phase was extracted with ether (3x)
  11. washthe combined organic extracts were washed with saturated sodium bicarbonate solution, saturated brine solution
  12. dry with materialdried over anhydrous magnesium sulphate
  13. customEvaporation of the solvent
  14. customyielded the crude product as a pale yellow oil
  15. distillationVacuum distillation

출처 및 근거

ORD 기록
ord-bf78a7c0cbc341b7b26a0654b5d987b7
출처 데이터셋
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04151179

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