Tetrahydrofuran → 3-Bromo-2-methyl-benzoic acid isopropyl ester

HRID 723021ノート

反応式

HRID 723021 の反応式
S(Cl)(Cl)=O.[Br:5][C:6]1[C:7]([CH3:15])=[C:8]([CH:12]=[CH:13][CH:14]=1)[C:9]([OH:11])=[O:10].[CH2:16]1[CH2:20]OC[CH2:17]1>C(Cl)Cl>[CH:16]([O:10][C:9](=[O:11])[C:8]1[CH:12]=[CH:13][CH:14]=[C:6]([Br:5])[C:7]=1[CH3:15])([CH3:20])[CH3:17]

参加物

5

反応物 3

HCID 8028TetrahydrofuranHCID 24386Thionyl ChlorideHCID 27355903-Bromo-2-methylbenzoic Acid

生成物 1

HCID 655448293-Bromo-2-methyl-benzoic acid isopropyl ester

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

Thionyl chloride (6 mL) was addend over 1 min to a 0° C. suspension of 3-bromo-2-methyl benzoic acid (2.15 g, 10 mmol) in DCM (10 mL). After 30 min of stirring, THF (5 mL) was added to induce dissolution. The now homogeneous solution was stirred for 24 h at rt and the volatile component were removed in vacuo. A portion of the crude acid chloride was dissolved in dry isopropyl alcohol (10 mL) and pyridine (2 mL) was added. After stirring for 4 h at rt, the volatile components were removed in vacuo. The residue was partitioned between EtOAc (70 mL) and HCl (1M, 30 mL) and the layers were separated. The organic layer was washed with HCl (1M, 10 mL), NaHCO3 (3×20 mL), water (30 mL), brine (30 mL), and was dried over sodium sulfate. Removal of solvent in vacuo yielded the title compound as a light-yellow oil which was used without further purification. 1H-NMR (CDCl3): δ 7.69 (d, 2H, J=7.7 Hz), 7.11 (t, 1H, J=7.9 Hz), 5.26 (heptet, 1H, J=6.3 Hz), 2.63 (s, 3H), 1.39 (d, 6H, J=6.3 Hz).

後処理

  1. dissolutiondissolution
  2. stirringThe now homogeneous solution was stirred for 24 h at rt
  3. customthe volatile component were removed in vacuo
  4. dissolutionA portion of the crude acid chloride was dissolved in dry isopropyl alcohol (10 mL)
  5. additionpyridine (2 mL) was added
  6. stirringAfter stirring for 4 h at rt
  7. customthe volatile components were removed in vacuo
  8. customThe residue was partitioned between EtOAc (70 mL) and HCl (1M, 30 mL)
  9. customthe layers were separated
  10. washThe organic layer was washed with HCl (1M, 10 mL), NaHCO3 (3×20 mL), water (30 mL), brine (30 mL)
  11. dry with materialwas dried over sodium sulfate
  12. customRemoval of solvent in vacuo

出典と根拠

ORDレコード
ord-f552375ed822416d871ea86156df9176
出典データセット
uspto-grants-2006_11
特許番号
US07138530B2

反応ノート

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