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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 178418435, 화합물 → HCID 178453956, 화합물

HRID 722029
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HRID 722029 반응식
B.[Na].[C:3]([O:7][C:8]([NH:10][C@H:11]1[CH2:16][CH2:15][C@H:14]([C:17](O)=[O:18])[CH2:13][CH2:12]1)=[O:9])([CH3:6])([CH3:5])[CH3:4]>O1CCCC1>[C:3]([O:7][C:8]([NH:10][C@H:11]1[CH2:12][CH2:13][C@H:14]([CH2:17][OH:18])[CH2:15][CH2:16]1)=[O:9])([CH3:6])([CH3:5])[CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 178418435HCID 178418435, 화합물HCID 178453972HCID 178453972, 화합물

생성물 1

HCID 178453956HCID 178453956, 화합물수율 53%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

9.33 g of sodium boron hydride was suspended in 200 ml of tetrahydrofuran, and added thereto was boron trifluoride diethyl complex under ice-cooling. The mixture was stirred as such under ice-cooling for 30 minutes, and then, 150 ml of a tetrahydrofuran solution containing 40 g of trans-4-(tert-butoxycarbonylamino)cyclohexane carboxylic acid was added thereto under ice-cooling. The mixture was stirred at room temperature for 4 hours, and the reaction mixture was poured into ice water, and extracted with chloroform. The extract was washed with water and brine, dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was recrystallized from ethyl acetate-hexane to obtain 20 g of N-tert-butoxycarbonyl-trans-4-(hydroxymethyl)cyclohexylamine.

후처리

  1. additionadded
  2. temperaturecooling
  3. temperaturecooling for 30 minutes
  4. additionwas added
  5. temperatureunder ice-cooling
  6. stirringThe mixture was stirred at room temperature for 4 hours
  7. extractionextracted with chloroform
  8. washThe extract was washed with water and brine
  9. dry with materialdried over anhydrous sodium sulfate
  10. customthe solvent was removed under reduced pressure
  11. customThe residue was recrystallized from ethyl acetate-hexane

출처 및 근거

ORD 기록
ord-d6ec5c4c5485463db101c3a7f8bc1b7b
출처 데이터셋
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07138397B2

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