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Ethyl Acetate → Ethyl 4-benzamido-3-oxopentanoate

HRID 46024
ノート
印刷プレビュー

反応式

HRID 46024 の反応式
[C:1]([NH:9][C@H:10]([C:12]([OH:14])=O)[CH3:11])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(C1NC=CN=1)(C1NC=CN=1)=O.[C:27]([O:30][CH2:31][CH3:32])(=[O:29])[CH3:28].[Li+].CC([N-]C(C)C)C>C1COCC1>[C:1]([NH:9][CH:10]([CH3:11])[C:12](=[O:14])[CH2:28][C:27]([O:30][CH2:31][CH3:32])=[O:29])(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8857Ethyl AcetateHCID 709778N-benzoyl-L-alanineHCID 2724682Lithium diisopropylamideHCID 5250894Bis-(1H-imidazol-2-YL)-methanone

生成物 1

HCID 21942725Ethyl 4-benzamido-3-oxopentanoate収率 95.5%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran
溶媒
2 回

実験手順

In the first flask, N-benzoylalanine (2 g, 10.35 mmol) was dissolved in THF (20 mL), and carbonyl diimidazole (CDI) (1.84 g, 11.39 mmol) was added. The resulting mixture was stirred 1 hour at rt and cooled down to −78° C. Into a second flask, ethyl acetate (3.83 g, 43.48 mmol) in THF (40 mL) was cooled down to −78° C. and LDA (24.3 mL, 48.51 mmol, 2 M in THF) pre-cooled to −78° C. was added. The resulting solution was stirred 30 minutes at −78° C., and the lithium enolate generated was cannulated into the first flask. The resulting white slurry was stirred 30 minutes at −78° C. and warmed up to −10° C. The reaction was quenched with a saturated aqueous solution of NH4Cl. Phases were separated and the organics were dried over MgSO4 and solvents removed under reduced pressure. The crude product was carried to the next step without purification. This gave ethyl 4-(benzoylamino)-3-oxopentanoate (2.6 g, 95.5% yield) as a white solid. ES-MS m/z 263.4 ((MH)+); HPLC RT (min.) 1.53; 1H NMR (Acetone-d6) δ 8.13 (s br, 1H), 7.93-7.91 (m, 2H), 7.58-7.43 (m, 3H), 4.72 (m, 1H), 4.19-4.01 (q, 2H), 3.67 (s, 2H), 1.47 (d, 3H), 1.15 (t, 3H).

後処理

  1. temperaturecooled down to −78° C
  2. additionwas added
  3. stirringThe resulting solution was stirred 30 minutes at −78° C.
  4. stirringThe resulting white slurry was stirred 30 minutes at −78° C.
  5. temperaturewarmed up to −10° C
  6. customThe reaction was quenched with a saturated aqueous solution of NH4Cl
  7. customPhases were separated
  8. dry with materialthe organics were dried over MgSO4 and solvents
  9. customremoved under reduced pressure
  10. customThe crude product was carried to the next step without purification

出典と根拠

ORDレコード
ord-ed1e17d9b44d40dfa50feb079b99c542
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08541618B2

反応ノート

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