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Ethyl Acetate → [(3S,5R)-5-(3,4,5-trifluorophenyl)morpholin-3-yl]methanol

HRID 16348
ノート
印刷プレビュー

反応式

HRID 16348 の反応式
Cl.C(OCC)(=O)C.C(OCC)(=O)C.C(OC(=O)[NH:20][C@@H:21]([CH2:36][O:37]CC1C=CC=CC=1)[CH2:22][O:23][CH2:24][C:25](=O)[C:26]1[CH:31]=[C:30]([F:32])[C:29]([F:33])=[C:28]([F:34])[CH:27]=1)(C)(C)C>[H][H]>[F:34][C:28]1[CH:27]=[C:26]([C@H:25]2[NH:20][C@@H:21]([CH2:36][OH:37])[CH2:22][O:23][CH2:24]2)[CH:31]=[C:30]([F:32])[C:29]=1[F:33]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8857Ethyl AcetateHCID 21866389Hydrogen chloride-ethyl acetateHCID 67373700tert-butyl {(S)-1-benzyloxymethyl-2-[2-oxo-2-(3,4,5-trifluorophenyl)ethoxy]ethyl}carbamate

生成物 1

HCID 67373759[(3S,5R)-5-(3,4,5-trifluorophenyl)morpholin-3-yl]methanol収率 78.5%

試薬・触媒・溶媒 1

HCID 178418361HCID 178418361、化合物溶媒

実験手順

A 4 N hydrochloric acid-ethyl acetate solution (30 mL) was added to an ethyl acetate solution (30 mL) of {(S)-1-benzyloxymethyl-2-[2-oxo-2-(3,4,5-trifluorophenyl)ethoxy]ethyl}carbamic acid tert-butyl ester (3.55 g) at room temperature. The resulting reaction solution was stirred at room temperature for 1 hr and then concentrated under reduced pressure. To a methanol solution (50 mL) of the obtained residue, 10% palladium-carbon (containing 50% water, 167 mg) was added. The resulting reaction solution was stirred in hydrogen atmosphere at room temperature for 18 hr, and the palladium carbon in the reaction solution was removed by filtration. The filtrate was concentrated under reduced pressure, and a saturated sodium hydrogencarbonate aqueous solution and ethyl acetate were added thereto. The organic layer was separated, washed with saturated saline, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluting solvent: heptane-ethyl acetate system) to give 1.52 g of the title compound. The physical property values of this compound were as follows:

後処理

  1. customThe resulting reaction solution
  2. concentrationconcentrated under reduced pressure
  3. additionTo a methanol solution (50 mL) of the obtained residue, 10% palladium-carbon (containing 50% water, 167 mg) was added
  4. customThe resulting reaction solution
  5. customthe palladium carbon in the reaction solution was removed by filtration
  6. concentrationThe filtrate was concentrated under reduced pressure
  7. additiona saturated sodium hydrogencarbonate aqueous solution and ethyl acetate were added
  8. customThe organic layer was separated
  9. washwashed with saturated saline
  10. dry with materialdried over anhydrous magnesium sulfate
  11. concentrationconcentrated under reduced pressure
  12. customThe residue was purified by silica gel column chromatography (eluting solvent: heptane-ethyl acetate system)

出典と根拠

ORDレコード
ord-6b19494e75424e0a9ec2808e38255079
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07737141B2

反応ノート

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