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Methanol → Methyl 3-iodo-alpha-methyl-D-phenylalaninate

HRID 857119
ノート
印刷プレビュー

反応式

HRID 857119 の反応式
[I:1][C:2]1[CH:3]=[C:4]([CH:12]=[CH:13][CH:14]=1)[CH2:5][C@:6]([CH3:11])([C:8]([OH:10])=[O:9])[NH2:7].S(Cl)(Cl)=O.[CH3:19]O>>[I:1][C:2]1[CH:3]=[C:4]([CH:12]=[CH:13][CH:14]=1)[CH2:5][C@:6]([CH3:11])([C:8]([O:10][CH3:19])=[O:9])[NH2:7]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 10357711H-alpha-Me-D-Phe(3-I)-OH

生成物 1

HCID 69344515Methyl 3-iodo-alpha-methyl-D-phenylalaninate

実験手順

A solution of 3-iodo-α-methyl-D-phenylalanine (0.9 g) in MeOH (50 ml) was treated with thionyl chloride (3.5 ml) and the mixture was heated to reflux for 3 days. The solvent was removed under reduced pressure and the residue was dissolved in EtOAc and washed with aqueous sodium bicarbonate, brine, dried (MgSO4) and evaporated to dryness to give the title compound (0.73 g) LCMS RT=2.12 min.

後処理

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 3 days
  3. customThe solvent was removed under reduced pressure
  4. dissolutionthe residue was dissolved in EtOAc
  5. washwashed with aqueous sodium bicarbonate, brine
  6. dry with materialdried (MgSO4)
  7. customevaporated to dryness

出典と根拠

ORDレコード
ord-2645e9c24a324bbf91119a7507b19592
出典データセット
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07144908B2

反応ノート

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