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Hydrochloric Acid → 3-(4-Fluoro-3-methoxyphenyl)prop-2-enoic acid

HRID 1593041
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HRID 1593041 반응식
[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][C:3]=1[O:10][CH3:11].C(O)(=O)[CH2:13][C:14]([OH:16])=[O:15].N1CCCCC1.Cl>N1C=CC=CC=1.O>[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[CH:13][C:14]([OH:16])=[O:15])=[CH:4][C:3]=1[O:10][CH3:11]
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참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 867Malonic AcidHCID 8082PiperidineHCID 27373584-Fluoro-3-methoxybenzaldehyde

생성물 1

HCID 534043133-(4-Fluoro-3-methoxyphenyl)prop-2-enoic acid수율 92%

시약·촉매·용매 2

HCID 962Water용매
HCID 1049
Pyridine
용매

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온도
85 °C

실험 절차

To a solution of 4-fluoro-3-methoxybenzaldehyde (32 g, 0.2 mol) in pyridine (100 mL) was added malonic acid (43 g, 0.4 mol) and piperidine (3 mL, 0.03 mol). The reaction solution was stirred at 85° C. for 13 hr. Upon cooling, the resulting suspension was added to cold water (500 mL) and acidified with conc. HCl (80 mL). The white solid was filtered off, washed with water and dried to yield 36 g (92%) of 3-(4-fluoro-3-methoxyphenyl)-acrylic acid. RP-HPLC: 3.71 min. 1H-NMR (DMSO-d6) δ (ppm) 3.85 (s, 3), 6.53 (d, 1, J=16), 7.20 (m, 2), 7.50 (m, 1), 7.52 (d, 1, J=16).

후처리

  1. temperatureUpon cooling
  2. filtrationThe white solid was filtered off
  3. washwashed with water
  4. customdried

출처 및 근거

ORD 기록
ord-3550d209127949a786385d4af8f367cb
출처 데이터셋
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07294635B2

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