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Methanol → Methyl 2-(4-cyano-2,5-difluorophenyl)acetate

HRID 1519528
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HRID 1519528 반응식
[C:1]([C:3]1[C:8]([F:9])=[CH:7][C:6]([CH2:10][C:11]([OH:13])=[O:12])=[C:5]([F:14])[CH:4]=1)#[N:2].S(Cl)(Cl)=O.[CH3:19]O>>[CH3:19][O:12][C:11](=[O:13])[CH2:10][C:6]1[CH:7]=[C:8]([F:9])[C:3]([C:1]#[N:2])=[CH:4][C:5]=1[F:14]
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참가 물질

4

반응물 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 675133414-Cyano-2,5-difluorophenylacetic acid

생성물 1

HCID 86694454Methyl 2-(4-cyano-2,5-difluorophenyl)acetate

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온도
85 °C

실험 절차

(4-Cyano-2,5-difluorophenyl)acetic acid (0.5 g, 2.5 mmol) was dissolved in methanol (20 mL), and thionyl chloride (0.5 mL) was added drop wise to the solution. The reaction was heated to 85° C. for 4 hours. Then it was cooled and evaporated to dryness in vacuo. The residue was partitioned between ethyl acetate and saturated NaHCO3. The organic layer was dried over MgSO4, filtered, and the filtrate was evaporated to dryness under reduced pressure to yield the title compound after purification on silica gel (eluted with 5-20% ethyl acetate-hexanes) as an off white solid. 1H NMR (500 MHz, CDCl3): δ 7.31 (dd, J=5.2, J=5.2 Hz, 1H), 7.19 (dd, J=5.7, J=5.8 Hz, 1H), 3.73 (s, 3H), 3.71 (s, 2H). LC-MS (IE, m/z): 212 [M+1]+.

후처리

  1. temperatureThen it was cooled
  2. customevaporated to dryness in vacuo
  3. customThe residue was partitioned between ethyl acetate and saturated NaHCO3
  4. dry with materialThe organic layer was dried over MgSO4
  5. filtrationfiltered
  6. customthe filtrate was evaporated to dryness under reduced pressure

출처 및 근거

ORD 기록
ord-0058fd27978b4e5eaf30f9c75f5535a5
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09073882B2

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