Water → 5-Ethoxypyrazine-2-carboxylic acid

HRID 1429624ノート

反応式

HRID 1429624 の反応式
[CH2:1]([O:3][C:4]1[N:5]=[CH:6][C:7]([C:10]([O:12]CC)=[O:11])=[N:8][CH:9]=1)[CH3:2].O.O.[OH-].[Li+].C([O-])(O)=O.[Na+]>O1CCOCC1.CCOCC>[CH2:1]([O:3][C:4]1[N:5]=[CH:6][C:7]([C:10]([OH:12])=[O:11])=[N:8][CH:9]=1)[CH3:2]

参加物

7

反応物 4

HCID 962WaterHCID 168937Lithium hydroxide, monohydrateHCID 516892Sodium BicarbonateHCID 668696851262803-60-0

生成物 1

HCID 574756925-Ethoxypyrazine-2-carboxylic acid

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 312751,4-Dioxane溶媒

実験手順

Ethyl 5-ethoxypyrazine-2-carboxylate (0.65 g, approx. purity 85%) was dissolved in dioxan (3 mL) and water (3 mL) was added, followed by lithium hydroxide monohydrate (255 mg, portionwise over 10 mins). After stirring at RT for 24h, Et2O (25 mL) and NaHCO3 (sat., aq., 25 mL) were added. The layers were separated and the organic layer was extracted with NaOH (1 N, aq., 25 mL). The combined aqueous portions were acidified with 6N HCl to pH 2, and the mixture extracted with EtOAc (3×40 mL). The combined EtOAc extracts were dried over MgSO4 and evaporated to afford the title compound as an off-white powder. 1H NMR (400 MHz, CDCl3) δ ppm 1.47 (t, J=7.1 Hz, 3 H), 4.53 (q, J=7.1 Hz, 2 H), 8.16 (d, J=1.2 Hz, 1 H), 8.98 (d, J=1.2 Hz, 1 H)

後処理

  1. additionwere added
  2. customThe layers were separated
  3. extractionthe organic layer was extracted with NaOH (1 N, aq., 25 mL)
  4. extractionthe mixture extracted with EtOAc (3×40 mL)
  5. dry with materialThe combined EtOAc extracts were dried over MgSO4
  6. customevaporated

出典と根拠

ORDレコード
ord-f2084eff099e4012873d50c5a2018109
出典データセット
uspto-grants-2015_01
特許番号
US08940734B2

反応ノート

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