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3-(4-Fluorophenyl)propionic acid → Methyl 3-(4-fluorophenyl)propanoate

HRID 1508553
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HRID 1508553 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][C:10]([OH:12])=[O:11])=[CH:4][CH:3]=1.[CH3:13][Si](C=[N+]=[N-])(C)C>C1(C)C=CC=CC=1.CO>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][C:10]([O:12][CH3:13])=[O:11])=[CH:6][CH:7]=1
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참가 물질

5

반응물 2

HCID 1363023-(4-Fluorophenyl)propionic acidHCID 167693Trimethylsilyldiazomethane

생성물 1

HCID 22906572Methyl 3-(4-fluorophenyl)propanoate

시약·촉매·용매 2

HCID 887Methanol용매HCID 1140Toluene용매

실험 절차

To a solution of 3-(4-fluorophenyl)propionic acid (4.75 g, 28.2 mmol) in toluene (130 mL) and methanol (20 mL) was added trimethylsilyldiazomethane (2M solution in hexane, 16.24 mL, 32.5 mmol). The mixture was allowed to stir for 1 hour and gas evolution was observed initially. After 1 hour, the mixture became homogeneous and was quenched via addition of 3.5 mL of acetic acid. The mixture was concentrated in vacuo, and purified via column chromatography on a Biotage 65i column eluting with 0% ethyl acetate in hexanes (1 CV) followed by a gradient to 50% ethyl acetate in hexanes (over 7 CV) to furnish the desired product. 1H NMR (CDCl3, 500 MHz) δ 7.16 (dd, J=8.0 Hz, 5.6 Hz, 2H), 6.97 (t, J=8.5 Hz, 2H), 3.66 (s, 3H), 2.92 (t, J=7.5 Hz, 2H), 2.61 (t, J=7.7 Hz, 2H).

후처리

  1. waitAfter 1 hour
  2. customwas quenched via addition of 3.5 mL of acetic acid
  3. concentrationThe mixture was concentrated in vacuo
  4. custompurified via column chromatography on a Biotage 65i column
  5. washeluting with 0% ethyl acetate in hexanes (1 CV)

출처 및 근거

ORD 기록
ord-5d94160db8c84f508a15f83e02dc9584
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09221834B2

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