Hydrochloric Acid → 2-(2-Amino-5-bromophenyl)propan-2-ol

HRID 2300093Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2300093
[NH2:1][C:2]1[CH:10]=[CH:9][C:8]([Br:11])=[CH:7][C:3]=1C(O)=O.[CH3:12][Mg].CC[O:16][CH2:17][CH3:18].Cl.[OH-].[Na+]>C1COCC1.C(OCC)(=O)C>[NH2:1][C:2]1[CH:10]=[CH:9][C:8]([Br:11])=[CH:7][C:3]=1[C:17]([OH:16])([CH3:18])[CH3:12]

Komponenten

8

Versuchsvorschrift

A solution of 2-amino-5-bromobenzoic acid (10 g, 46 mmol) in dry THF (200 mL) was treated at −78° C. under nitrogen with a solution of methylmagnesium brormide in ether (3.0 M, 90 mL, 270 mmol). The reaction mixture was slowly warmed to ambient temperature, kept stirring for 48 hours under nitrogen and then poured into a cold 0.5 N aqueous hydrochloride solution (300 mL). The mixture was neutralized with aqueous 1 N sodium hydroxide solution and ethyl acetate (300 mL) was added. The organic layer was separated and aqueous layer was extracted with ethyl acetate (3×100 mL). The combined organic layers were washed with brine and dried (MgSO4). After removal of solvent in vacuo, the residue was purified by a silica gel flash column chromatography(hexane:ethyl acetate/3:2) to give 2-(2-amino-5-bromophenyl)propan-2-ol as off-white solid (6 g, 57%): mp 62-63° C.; 1H-NMR (CDCl3) δ 7.19 (d, 1H, J=2.3 Hz), 7.12 (dd, 1H, J=8.4, 2.3 Hz), 6.51 (d, 1H, J=8.4 Hz), 4.70 (s, 2H), 1.82 (s, 1H), 1.65 (s, 6H).

Aufarbeitung

  1. additionwas added
  2. customThe organic layer was separated
  3. extractionaqueous layer was extracted with ethyl acetate (3×100 mL)
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried (MgSO4)
  6. customAfter removal of solvent in vacuo
  7. customthe residue was purified by a silica gel flash column chromatography(hexane:ethyl acetate/3:2)

Quellen und Nachweise

ORD-Eintrag
ord-ae1529e2adeb4a6c879c85bf0c50863c
Quelldatensatz
uspto-grants-2002_12
Patentnummer
US06498154B1

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