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Triphenylphosphine → Tert-butyl 1-oxa-8-azaspiro[4.5]decane-8-carboxylate

HRID 2213016
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HRID 2213016 반응식
CCOC(/N=N/C(OCC)=O)=O.O[C:14]1([CH2:27][CH2:28][CH2:29][OH:30])[CH2:19][CH2:18][N:17]([C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])[CH2:16][CH2:15]1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>O1CCCC1>[O:30]1[C:14]2([CH2:15][CH2:16][N:17]([C:20]([O:22][C:23]([CH3:24])([CH3:25])[CH3:26])=[O:21])[CH2:18][CH2:19]2)[CH2:27][CH2:28][CH2:29]1
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참가 물질

5

반응물 3

HCID 11776TriphenylphosphineHCID 5462977Diethyl azodicarboxylateHCID 21955351HCID 21955351, 화합물

생성물 1

HCID 21955197Tert-butyl 1-oxa-8-azaspiro[4.5]decane-8-carboxylate수율 74%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
0 °C

실험 절차

A solution of diethyl diazenedicarboxylate (3.35 mL, 21.3 mmol) in tetrahydrofuran (50 mL) was added over 15 minutes to a stirred, cooled (0° C.) solution of 1,1-dimethylethyl 4-hydroxy-4-(3-hydroxypropyl)-1-piperidinecarboxylate (Description 73, 4.6 g, 17.8 mmol) and triphenylphosphine (5.58 g, 21.3 mmol) in tetrahydrofuran (150 mL) and the mixture was stirred at 0° C. for 1 hour, then at room temperature for 24 hours. The solvent was evaporated under reduced pressure and the residue was purified by flash column chromatography on silica gel, eluting with isohexane/EtOAc (75:25 increasing to 50:50), to give the title compound (3.18 g, 70%). m/z (ES+) 242 (M+1).

후처리

  1. waitat room temperature for 24 hours
  2. customThe solvent was evaporated under reduced pressure
  3. customthe residue was purified by flash column chromatography on silica gel
  4. washeluting with isohexane/EtOAc (75:25 increasing to 50:50)

출처 및 근거

ORD 기록
ord-31c7bb5c8a9245d3890139f9ada9aac4
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07105507B2

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