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Methanol → Methyl 3-(5-hydroxypyrimidin-2-yl)benzoate

HRID 1970876
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HRID 1970876 반응식
S(Cl)(Cl)=O.[OH:5][C:6]1[CH:7]=[N:8][C:9]([C:12]2[CH:13]=[C:14]([CH:18]=[CH:19][CH:20]=2)[C:15]([OH:17])=[O:16])=[N:10][CH:11]=1.[CH3:21]O>>[OH:5][C:6]1[CH:11]=[N:10][C:9]([C:12]2[CH:13]=[C:14]([CH:18]=[CH:19][CH:20]=2)[C:15]([O:17][CH3:21])=[O:16])=[N:8][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 887MethanolHCID 24386Thionyl Chloride3회HCID 594849363-(5-Hydroxypyrimidin-2-yl)benzoic acid

생성물 1

HCID 59438048Methyl 3-(5-hydroxypyrimidin-2-yl)benzoate

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온도
80 °C

실험 절차

32.7 ml (445 mmol) of thionyl chloride are added to a suspension of 88.0 g (366 mmol) of 3-(5-hydroxypyrimidin-2-yl)benzoic acid in 1.41 of methanol, and the mixture is heated at 80° C. for 2 hours. 20 ml (276 mmol) of thionyl chloride and, after 2 hours, a further 10 ml (138 mmol) of thionyl chloride are then added. After each addition, the reaction mixture is stirred at 80° C. for 2 hours. The reaction mixture is concentrated to a volume of about 300 ml in vacuo. The resultant precipitate is filtered off and dried in vacuo: methyl 3-(5-hydroxypyrimidin-2-yl)benzoate as brownish crystals; m.p. 219-223° C., ESI 231 (M+H); HPLC: Rt=3.87 min (method C).

후처리

  1. additionAfter each addition
  2. concentrationThe reaction mixture is concentrated to a volume of about 300 ml in vacuo
  3. filtrationThe resultant precipitate is filtered off
  4. customdried in vacuo

출처 및 근거

ORD 기록
ord-9730e458a3584ca4a6940f2c9c5e9224
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08431572B2

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