Water → ((2-Thienylcarbonyl)amino)acetic acid

HRID 1178074

反応式

HRID 1178074 の反応式
O[Li].O.C([O:6][C:7](=[O:17])[CH2:8][NH:9][C:10]([C:12]1[S:13][CH:14]=[CH:15][CH:16]=1)=[O:11])C.C1COCC1.O>CO>[S:13]1[CH:14]=[CH:15][CH:16]=[C:12]1[C:10]([NH:9][CH2:8][C:7]([OH:17])=[O:6])=[O:11]

参加物

6

反応物 4

HCID 962WaterHCID 8028TetrahydrofuranHCID 168937Lithium hydroxide, monohydrateHCID 1720748Ethyl N-(thiophene-2-carbonyl)glycinate

生成物 1

HCID 679227((2-Thienylcarbonyl)amino)acetic acid収率 70%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

LiOH.H2O (110 mg, 2.63 mmol) was added to a solution of [(thiophene-2-carbonyl)-amino]-acetic acid ethyl ester (140 mg, 0.66 mmol) in a mixture of MeOH (5 mL), THF (2.5 mL) and H2O (2.5 mL). The resulting mixture was stirred for 3 hrs at room temperature. The MeOH and THF were evaporated and the resulting residue was diluted with water (2 mL), acidified with citric acid and extracted with EtOAc. The organic layer was washed with brine solution, dried over Na2SO4 and concentrated under reduced pressure to afford [(thiophene-2-carbonyl)-amino]-acetic acid in 70% yield. LC-MS purity: 92%.

後処理

  1. customThe MeOH and THF were evaporated
  2. additionthe resulting residue was diluted with water (2 mL)
  3. extractionextracted with EtOAc
  4. washThe organic layer was washed with brine solution
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-019afa39c9b64df397d52169620cad22
出典データセット
uspto-grants-2010_11
特許番号
US07842696B2

関連ノート

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