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Sodium Hydroxide → HCID 15614980, 화합물

HRID 620226
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HRID 620226 반응식
[C:1]([NH:11][C@H:12]([C:14]([N:16]([C:23]1[CH:24]=[C:25]2[C:29](=[CH:30][CH:31]=1)[CH2:28][CH2:27][CH2:26]2)[CH2:17][C:18]([O:20]CC)=[O:19])=[O:15])[CH3:13])([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:2].[OH-].[Na+]>C(O)C>[C:1]([NH:11][C@H:12]([C:14]([N:16]([C:23]1[CH:24]=[C:25]2[C:29](=[CH:30][CH:31]=1)[CH2:28][CH2:27][CH2:26]2)[CH2:17][C:18]([OH:20])=[O:19])=[O:15])[CH3:13])([O:3][CH2:4][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1)=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 15614978HCID 15614978, 화합물

생성물 1

HCID 15614980HCID 15614980, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of ethyl N-carbobenzoxy-L-alanyl-N-(5-indanyl)-glycinate (14.0 g, 33.0 mmol) in 150 ml ethanol was added sodium hydroxide (25 ml of a 2N aqueous solution, 49.5 mmol) and mixture stirred at room temperature for 20 h. The volatiles were removed under reduced pressure and the residue dissolved in ether and saturated sodium bicarbonate. The organic layer was separated and extracted with saturated sodium bicarbonate. The combined basic extracts were cooled in an ice bath and acidified with concentrated HCl. The aqueous solution was extracted thoroughly with CH2Cl2. The combined organic extracts were dried (MgSO4) and concentrated in vacuo.

후처리

  1. customThe volatiles were removed under reduced pressure
  2. dissolutionthe residue dissolved in ether
  3. customThe organic layer was separated
  4. extractionextracted with saturated sodium bicarbonate
  5. temperatureThe combined basic extracts were cooled in an ice bath
  6. extractionThe aqueous solution was extracted thoroughly with CH2Cl2
  7. dry with materialThe combined organic extracts were dried (MgSO4)
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-da701ad6601d4ca19cfee56ecda277b5
출처 데이터셋
uspto-grants-1989_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04820729

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