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Water → tert-Butyl (2S)-2-(hydroxymethyl)piperidine-1-carboxylate

HRID 1909677
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HRID 1909677 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH2:11][CH2:10][C@H:9]1[C:14](O)=[O:15])=[O:7])([CH3:4])([CH3:3])[CH3:2].B.O1CCCC1.O>C1COCC1>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH2:11][CH2:10][C@H:9]1[CH2:14][OH:15])=[O:7])([CH3:4])([CH3:3])[CH3:2]
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참가 물질

5

반응물 3

HCID 962WaterHCID 688617(2S)-1-((tert-butoxy)carbonyl)piperidine-2-carboxylic acidHCID 2723981Borane;tetrahydrofuran

생성물 1

HCID 6933954tert-Butyl (2S)-2-(hydroxymethyl)piperidine-1-carboxylate수율 100.6%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
2.5 °C

실험 절차

To a solution of (S)-Piperidine-1,2-dicarboxylic acid 1-tert-butyl ester (5 g, 21.8 mmol) in anhydrous THF (32 mL) at 0-5° C. was added borane-tetrahydrofuran complex (1M solution in THF) (3.6 g, 41.84 mmol) over a period of 15 min. The mixture was stirred at 0-5° C. for 2 h and then at rt for 2 h. The mixture was added over a period of 10 min to cold water (75 mL) and extracted with EtOAc (300 mL). The aqueous layer was re-extracted with EtOAc (2×150 mL). The organic layers were combined, dried over anhydrous Na2SO4 and concentrated to obtain the title product as a colorless oil (4.72 g).

후처리

  1. waitat rt for 2 h
  2. extractionextracted with EtOAc (300 mL)
  3. extractionThe aqueous layer was re-extracted with EtOAc (2×150 mL)
  4. dry with materialdried over anhydrous Na2SO4
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-33daebbf351a4f298075baec8676ddfd
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08598359B2

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