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Hydrochloric Acid → HCID 23251676、化合物

HRID 2044023
ノート
印刷プレビュー

反応式

HRID 2044023 の反応式
[CH2:1]([O:8][C:9](=[O:24])[CH:10]([NH:16][C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])[CH2:11][CH2:12][C:13](O)=[O:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(OC(Cl)=O)C.[BH4-].[Na+].Cl>C1COCC1.O>[CH2:1]([O:8][C:9](=[O:24])[CH:10]([NH:16][C:17]([O:19][C:20]([CH3:22])([CH3:21])[CH3:23])=[O:18])[CH2:11][CH2:12][CH2:13][OH:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 10928Ethyl chloroformateHCID 3255276Boc-D-glutamic acid 1-benzyl esterHCID 4311764Sodium borohydride

生成物 1

HCID 23251676HCID 23251676、化合物収率 75%

試薬・触媒・溶媒 2

HCID 962Water触媒
HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
0 °C

実験手順

The 2-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester (4.06 g, 12 mmol) and TEA (5 mL, 35.87 mmol) were dissolved in THF (60 mL) and cooled to 0° C. Ethylchloroformate (3.4 mL, 35.7 mmol) was added dropwise. The mixture was stirred at 0° C. for 5 minutes and warmed to r.t. for 1 h. NaBH4 (1.88 g, 49.7 mmol) was added followed by addition of 1 drop of H2O. The reaction mixture was stirred at r.t. overnight. 4 N HCl was added at 0° C. and extracted with EtOAc (100 mL). The aqueous layer was washed with H2O (100 mL), NaOH (2×100 mL), H2O (100 mL) and brine (100 mL). The organic layer was dried with Na2SO4, filtered, and concentrated. The crude product was purified by combi-flash to give 2.89 g of 2-tert-butoxycarbonylamino-5-hydroxy-pentanoic acid benzyl ester in 75% yield.

後処理

  1. temperaturewarmed to r.t. for 1 h
  2. stirringThe reaction mixture was stirred at r.t. overnight
  3. extractionextracted with EtOAc (100 mL)
  4. washThe aqueous layer was washed with H2O (100 mL), NaOH (2×100 mL), H2O (100 mL) and brine (100 mL)
  5. dry with materialThe organic layer was dried with Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe crude product was purified by combi-flash

出典と根拠

ORDレコード
ord-00fe12ce2d874490b84dde1d698bf087
出典データセット
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08586744B2

反応ノート

読み込み中…

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