Trimethyl orthoformate → Tert-butyl 3,3-dimethoxycyclopentanecarboxylate

HRID 1816959ノート

反応式

HRID 1816959 の反応式
O=[C:2]1C[CH2:5][CH:4]([C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[CH2:3]1.CO[CH:16]([O:19][CH3:20])[O:17][CH3:18]>CC1C=CC(S(O)(=O)=O)=CC=1.O.C(Cl)Cl.CO>[CH3:20][O:19][C:16]1([O:17][CH3:18])[CH2:2][CH2:3][CH:4]([C:7]([O:9][C:10]([CH3:12])([CH3:11])[CH3:13])=[O:8])[CH2:5]1

参加物

5

反応物 2

HCID 9005Trimethyl orthoformateHCID 14009986tert-Butyl 3-oxocyclopentane-1-carboxylate

生成物 1

HCID 58784445Tert-butyl 3,3-dimethoxycyclopentanecarboxylate収率 90.1%

試薬・触媒・溶媒 2

HCID 521998p-Toluenesulfonic acid monohydrate触媒2 回HCID 21226129Dichloromethane methanol溶媒

実験手順

To a solution of tert-butyl 3-oxocyclopentanecarboxylate (19.8 g, 107 mmol) in 1:1 DCM/methanol (150 mL) was added trimethylorthoformate (46.8 mL, 428 mmol), followed by TsOH.H2O (˜0.5 g). The reaction mixture was stirred at room temperature for 2 h. Then more TsOH.H2O (˜0.25 g) was added and the reaction mixture was stirred overnight. The reaction mixture was concentrated at room temperature and the resulting residue was dissolved in ether and washed with saturated NaHCO3 solution, then with brine. The ethereal layer was dried over anhydrous MgSO4, filtered, and concentrated. Purification by flash chromatography (silica, 15% ethyl acetate/hexane) gave 22.2 g (90%) of tert-butyl 3,3-dimethoxycyclopentanecarboxylate.

後処理

  1. stirringthe reaction mixture was stirred overnight
  2. concentrationThe reaction mixture was concentrated at room temperature
  3. dissolutionthe resulting residue was dissolved in ether
  4. washwashed with saturated NaHCO3 solution
  5. dry with materialThe ethereal layer was dried over anhydrous MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customPurification by flash chromatography (silica, 15% ethyl acetate/hexane)

出典と根拠

ORDレコード
ord-54082dc2ff724e2185a44c42f5c845fa
出典データセット
uspto-grants-2009_10
特許番号
US07598243B2

反応ノート

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