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Benzenepropanoyl chloride → HCID 12112436, Verbindung

HRID 1838058
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1838058
[NH2:1][C:2]1[CH:9]=[C:8]([F:10])[CH:7]=[CH:6][C:3]=1[CH2:4][OH:5].C(N(CC)C(C)C)(C)C.[C:20](Cl)(=[O:29])[CH2:21][CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>C(Cl)Cl>[F:10][C:8]1[CH:7]=[CH:6][C:3]([CH2:4][OH:5])=[C:2]([NH:1][C:20](=[O:29])[CH2:21][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH:9]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 64801Benzenepropanoyl chlorideHCID 81531DiisopropylethylamineHCID 12737325(2-Amino-4-fluorophenyl)methanol

Produkt 1

HCID 12112436HCID 12112436, VerbindungAusbeute 87,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

To a solution of 2-amino-4-fluorobenzyl alcohol from Step 1 (2.00 g, 14.17 mmol) and methylene chloride (45 mL), was added N,N,-diisopropylethylamine (3.70 g, 28.34 mmol) followed by hydrocinnamoyl chloride (4.78 g, 28.34 mmol) dropwise over 15 min under an argon atmosphere at 23° C. After 16 h, the reaction was diluted with methylene chloride (100 mL), washed with KHSO4 (1 N, 1×80 mL), sat'd NaHCO3 (1×80 mL), brine (1×80 mL) and dried (MgSO4). After concentration in vacuo, the crude residue was dissolved in methanol (14 mL) and NaOH (1.5 N, 14 mL) was added at 23° C. under argon. After 2 h at 23° C., the reaction was concentrated in vacuo, diluted with ether (150 mL), washed with brine (100 mL), and dried (MgSO4). After concentration in vacuo, the residue was purified by flash chromatography (ethyl acetate:hexane 1:3) to afford N-[5-fluoro-2-hydroxymethylphenyl]benzenepropanamide (3.40 g, 87.8%) as an oil: 1H NMR (CDCl3) δ 2.65 (t, J=7 Hz), 3.05 (t, J=7 Hz), 4.48 (s), 6.68-6.74 (m), 7.00-7.34 (m), 7.83-7.91 (m) 8.72 (br s). MS (EI) 273, 255, 212. IR (neat) 3500-3150, 1667 cm−1. Anal. Calc'd. for C16H16NO2F: C, 70.31; H, 5.90; N, 5.13. Found: C, 70.26; H, 6.11; N, 5.03.

Aufarbeitung

  1. washwashed with KHSO4 (1 N, 1×80 mL), sat'd NaHCO3 (1×80 mL), brine (1×80 mL)
  2. dry with materialdried (MgSO4)
  3. concentrationAfter concentration in vacuo
  4. dissolutionthe crude residue was dissolved in methanol (14 mL)
  5. additionNaOH (1.5 N, 14 mL) was added at 23° C. under argon
  6. waitAfter 2 h at 23° C.
  7. concentrationthe reaction was concentrated in vacuo
  8. additiondiluted with ether (150 mL)
  9. washwashed with brine (100 mL)
  10. dry with materialdried (MgSO4)
  11. concentrationAfter concentration in vacuo
  12. customthe residue was purified by flash chromatography (ethyl acetate:hexane 1:3)

Quellen und Nachweise

ORD-Eintrag
ord-2d5bde31e77f4ea98fdf6aa8b64bf363
Quelldatensatz
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06673784B1

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