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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Norleucine, D-(-)- → Hexanoic acid, 2-hydroxy-, (2R)-

HRID 890681
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HRID 890681 반응식
N[C@@H:2]([C:7]([OH:9])=[O:8])[CH2:3][CH2:4][CH2:5][CH3:6].N([O-])=[O:11].[Na+]>S(=O)(=O)(O)O.O>[OH:11][C@H:2]([CH2:3][CH2:4][CH2:5][CH3:6])[C:7]([OH:9])=[O:8]
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참가 물질

5

반응물 2

HCID 456468Norleucine, D-(-)-HCID 23668193Sodium Nitrite

생성물 1

HCID 6995511Hexanoic acid, 2-hydroxy-, (2R)-

시약·촉매·용매 2

HCID 962Water용매HCID 1118Sulfuric Acid용매

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온도
0 °C

실험 절차

To a cooled (0° C.), stirred solution of D-norleucine (500 mg, 3.81 mmol) in 10 mL of 1N aqueous sulfuric acid was added sodium nitrite (421 mg, 6.10 mmol) in 3 mL of water dropwise over a 20-minute period. The reaction mixture was allowed to slowly warm to room temperature over a 16-hour period. The mixture then was extracted with EtOAc (2×25 mL), dried (Na2SO4), and concentrated to yield 200 mg (40%) of a white waxy solid.

후처리

  1. temperatureto slowly warm to room temperature over a 16-hour period
  2. extractionThe mixture then was extracted with EtOAc (2×25 mL)
  3. dry with materialdried (Na2SO4)
  4. concentrationconcentrated
  5. customto yield 200 mg (40%) of a white waxy solid

출처 및 근거

ORD 기록
ord-179b506ce4f74a2ca29ba9e4692847d9
출처 데이터셋
uspto-grants-2006_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06998416B2

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