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Sulfuric Acid → tert-Butyl propionate

HRID 1005396
ノート
印刷プレビュー

反応式

HRID 1005396 の反応式
[CH3:1]C(C1C=CC(CBr)=CC=1)(S(OCC)(=O)=O)C.[C:18]([O:22][C:23](=[O:39])[CH2:24]N=C(C1C=CC=CC=1)C1C=CC=CC=1)([CH3:21])([CH3:20])[CH3:19].C[Si]([N-][Si](C)(C)C)(C)C.[Na+].ClC(OCC1C=CC=CC=1)=O.OS(O)(=O)=O>C1COCC1.O>[C:18]([O:22][C:23](=[O:39])[CH2:24][CH3:1])([CH3:21])([CH3:20])[CH3:19]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 1118Sulfuric AcidHCID 10387Benzyl chloroformateHCID 688171N-(Diphenylmethylene)glycine tert-butyl esterHCID 2724254Sodium bis(trimethylsilyl)amideHCID 21706518Ethyl 1-methyl-1-(4-bromomethylphenyl)ethanesulfonate

生成物 1

HCID 88561tert-Butyl propionate収率 250.2%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of ethyl 1-methyl-1-(4-bromomethylphenyl)ethanesulfonate (0.64 g, 1.89 mol) and N-diphenylmethyleneglycine t butyl ester (0.586 g, 1.98 mmol) in THF (6.5 mL) cooled on ice was added sodium bis(trimethylsilyl)amide (2M in THF, 1.04 mL). After 30 minutes the solvent was evaporated, the residue was taken up in acetic acid (2 mL), water (2 mL) and methanol (4 mL), and stirred at rt for 4 hours. The methanol was evaporated, water was added, and the mixture was washed with hexane/ether 1/1 (2×20 mL). The organic phase was washed with water. The combined aqueous phase was cooled on ice, and adjusted to pH 7 with sodium bicarbonate. Dioxane was added followed by benzyl chloroformate (0.38 mL, 2.65 mmol) and the mixture was stirred coming to rt overnight. Water was added, and the mixture was acidified to pH 3 with 1N H2SO4. The mixture was extracted with ethyl acetate, and the organic phase was dried, filtered and evaporated. Chromatography of the residue over silica gel (10% to 20% ethyl acetate/hexane) gave crude 2-(R,S)-benzyloxycarbonylamino-3-[4'-(1"-ethyloxysulfonyl-1"-methyl)ethyl)benzene]propanoic acid t butyl ester (0.645 g, 68%). To a solution of the crude ester in methylene chloride (9 mL) cooled on ice was added trifluoroacetic acid (1.5 mL). The mixture was stirred for 4 hours, warming to rt. The reaction was quenched with cold aqueous sodium bicarbonate, and extracted with methylene chloride. The solvent was evaporated, and chromatography of the residue over silica gel (methylene chloride to 10% methanol/methylene chloride) gave 2-(R,S)-benzyloxycarbonylamino-3-[4'-(1"-ethyloxysulfonyl-1"-methyl)ethyl)benzene]propanoic acid (0.396 g, 0.88 mmol, 69%).

後処理

  1. customAfter 30 minutes the solvent was evaporated
  2. customThe methanol was evaporated
  3. additionwater was added
  4. washthe mixture was washed with hexane/ether 1/1 (2×20 mL)
  5. washThe organic phase was washed with water
  6. temperatureThe combined aqueous phase was cooled on ice
  7. additionDioxane was added
  8. stirringthe mixture was stirred
  9. waitcoming to rt overnight
  10. extractionThe mixture was extracted with ethyl acetate
  11. customthe organic phase was dried
  12. filtrationfiltered
  13. customevaporated

出典と根拠

ORDレコード
ord-bf5f38abc0a74a1e919f07fdbe9513ea
出典データセット
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06054470

反応ノート

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