Methanol → 1-Naphthylglycine methyl ester hydrochloride

HRID 2242546ノート

反応式

HRID 2242546 の反応式
S(Cl)([Cl:3])=O.[C:5]1([NH:15][CH2:16][C:17]([OH:19])=[O:18])[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[CH:7][CH:6]=1.[CH3:20]O>C(OCC)C>[ClH:3].[CH3:20][O:18][C:17](=[O:19])[CH2:16][NH:15][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[CH:7][CH:6]=1

参加物

5

反応物 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 4587031-Naphthylglycine

生成物 1

HCID 668078681-Naphthylglycine methyl ester hydrochloride収率 98%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

33 mL of thionyl chloride was added dropwise to a mixture of 50.3 g of 1-naphthylglycine (racemic modification) and 200 mL of methanol (dehydrated) at an inner temperature of 35° C. over 1 hour and the mixture was stirred at the same temperature for 3 hours to effect reaction. The reaction mixture was concentrated and the concentrated residue obtained was mixed with 200 mL of diethyl ether. Then, the crystals produced were isolated by filtration and washed with 50 mL of diethyl ether. The crystals isolated by filtration were dried at an inner temperature of 50° C. under reduced pressure to obtain 61.9 g of ochre 1-naphthylglycine methyl ester hydrochloride (yield: 98%).

後処理

  1. customreaction
  2. concentrationThe reaction mixture was concentrated
  3. customthe concentrated residue obtained
  4. customThen, the crystals produced
  5. customwere isolated by filtration
  6. washwashed with 50 mL of diethyl ether
  7. customThe crystals isolated by filtration
  8. customwere dried at an inner temperature of 50° C. under reduced pressure

出典と根拠

ORDレコード
ord-8d75b1f296d749f884489c2d36d4f49b
出典データセット
uspto-grants-2010_03
特許番号
US07671213B2

反応ノート

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