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Methanol → Ethyl N-(methoxycarbonyl)glycinate

HRID 2412316
ノート
印刷プレビュー

反応式

HRID 2412316 の反応式
Cl.[CH2:2]([O:4][C:5](=[O:8])[CH2:6][NH2:7])[CH3:3].[CH3:9][OH:10].[N-]=[C:12]=[O:13]>O1CCCC1>[CH2:2]([O:4][C:5](=[O:8])[CH2:6][NH:7][C:9]([O:13][CH3:12])=[O:10])[CH3:3]
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 887MethanolHCID 105034IsocyanateHCID 2723640Glycine ethyl ester, hydrochloride

生成物 1

HCID 235150Ethyl N-(methoxycarbonyl)glycinate

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Alternatively, glycine ethyl ester hydrochloride (40.1 g, 0.28 mole) suspended in dry tetrahydrofuran (200 ml) and phosgene were bubbled through the reaction mixture for 0.5 hrs, as the reaction mixture was refluxed. At the end of 0.5 hrs., the reaction was cooled to room temperature and toluene was added followed by the distillation of THF. The reaction mixture containing toluene was further refluxed for 1 hr. The unreacted glycine ethyl ester hydrochloride was filtered and the filtrate containing glycine ethyl ester isocyanate (IR 2250 cm-1) was reacted with excess (2-3 mole) anhydrous methanol and, when the isocyanate peak disappeared, the solvent was removed to isolate N-carbomethoxyglycine ethyl ester.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customphosgene were bubbled through the reaction mixture for 0.5 hrs, as the reaction mixture
  2. temperaturewas refluxed
  3. customAt the end of 0.5 hrs
  4. additiontoluene was added
  5. distillationfollowed by the distillation of THF
  6. additionThe reaction mixture containing toluene
  7. temperaturewas further refluxed for 1 hr
  8. filtrationThe unreacted glycine ethyl ester hydrochloride was filtered
  9. additionthe filtrate containing glycine ethyl ester isocyanate (IR 2250 cm-1)
  10. customthe solvent was removed

出典と根拠

ORDレコード
ord-c2e26164a4814f2490e474bd28d0bc9a
出典データセット
uspto-grants-1985_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04491548

反応ノート

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