Tetrahydrofuran → HCID 67041804、化合物

HRID 62766ノート

反応式

HRID 62766 の反応式
Cl[C:2]1[CH:3]=[C:4]([CH:18]=[C:19]([Cl:22])[C:20]=1[OH:21])C(NC1C=CC(C(OC)=O)=CC=1)=O.[CH2:23]([Li])CCC.Cl[C:29]([O:31][CH2:32][CH3:33])=[O:30].C1C[O:37][CH2:36]C1>>[Cl:22][C:19]1[C:20]([O:21][CH3:23])=[CH:2][C:3]([C:29]([O:31][CH2:32][CH3:33])=[O:30])=[CH:4][C:18]=1[O:37][CH3:36]

参加物

5

反応条件

温度
-70 °C

実験手順

A solution of 2-chloro-5-iodo-1,3-dimethoxybenzene (1) (3.4 g, 11 mmol) in anhydrous THF (100 mL) was cooled to −70° C. and treated with n-butyllithium (5.5 mL, 12 mmol). The reaction mixture was stirred at −70° C. for 45 min then ethyl chloroformate (1.6 mL, 17 mmol) was added dropwise and the reaction mixture was allowed to warm to RT and stirred for 20 h. The reaction mixture was poured on to ice (100 mL) and the product was extracted with EtOAc (2×100 mL). The organic solution was washed with brine (3×100 mL) and the solvent was removed in vacuo. The residue was purified by silica gel chromatography (120 g, 0-50% EtOAc in isohexane) to afford ethyl 4-chloro-3,5-dimethoxybenzoate (2) (0.12 g, 4%): 1H NMR (400 MHz, CDCl3) δ: 7.30 (2H, s), 4.40 (2H, q), 3.96 (6H, s), 1.42 (3H, t).

後処理

  1. temperatureto warm to RT
  2. stirringstirred for 20 h
  3. extractionthe product was extracted with EtOAc (2×100 mL)
  4. washThe organic solution was washed with brine (3×100 mL)
  5. customthe solvent was removed in vacuo
  6. customThe residue was purified by silica gel chromatography (120 g, 0-50% EtOAc in isohexane)

出典と根拠

ORDレコード
ord-2116a5c7a805481dbd816b244979f35e
出典データセット
uspto-grants-2016_09
特許番号
US09447028B2

反応ノート

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