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Hexane → HCID 69221993, 화합물

HRID 901463
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HRID 901463 반응식
[Br-].[CH2:2]([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[CH2:3][CH3:4].[CH3:24]CCCCC.[H-].[Na+].[C:32]([O:36][C:37]([N:39]1[CH2:44][CH2:43][C:42](=O)[CH2:41][CH:40]1[C:46]([OH:48])=[O:47])=[O:38])([CH3:35])([CH3:34])[CH3:33]>C1COCC1.O>[CH3:24][O:48][C:46]([CH:40]1[CH2:41][C:42](=[CH:2][CH2:3][CH3:4])[CH2:43][CH2:44][N:39]1[C:37]([O:36][C:32]([CH3:35])([CH3:34])[CH3:33])=[O:38])=[O:47]
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참가 물질

7

반응물 4

HCID 8058HexaneHCID 24758Sodium hydrideHCID 80374Propyltriphenylphosphonium bromideHCID 468356941-(tert-Butoxycarbonyl)-4-oxopiperidine-2-carboxylic acid

생성물 1

HCID 69221993HCID 69221993, 화합물

시약·촉매·용매 2

HCID 962Water용매
HCID 8028
Tetrahydrofuran
용매
3회

실험 절차

Propyltriphenylphosphonium bromide (1.24 g, 3.22 mmol) in THF (10 mL) was added to hexane washed sodium hydride (123 mg, 3.22 mmol), in THF (10 mL) and stirred at room temperature for 3 h. Methyl ester 12a (P=Boc, m=2, P2=Me) (0.55 g, 2.15 mmol) in THF (5 mL) was added to the above reaction mixture slowly and then allowed to stir for additional 2 h. It was then poured into water and extracted with ethyl acetate (30 mL). The organic phase was dried with magnesium sulfate, filtered and evaporated to dryness, the resulting residue was chromatographed using 20% EtOAc in hexanes to provide the product 4-propylidene-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester. (0.100 g, 16%): MS (ESPOS): 284 [M+H]+; 1H NMR (300 MHz, CD3OD) δ 5.18 (m, m), 4.60-4.93 (m, 1), 3.91 (m, 1), 3.67 (s, 3), 2.94-3.04 (m, 2), 2.40-2.48 (m, 2), 1.99-2.06 (m, 1), 1.85-1.97 (m, 2), 1.38 (bs, 9), 0.85 (t, J=5 Hz, 3).

후처리

  1. extractionextracted with ethyl acetate (30 mL)
  2. dry with materialThe organic phase was dried with magnesium sulfate
  3. filtrationfiltered
  4. customevaporated to dryness
  5. customthe resulting residue was chromatographed

출처 및 근거

ORD 기록
ord-18f4c0287e114006a64480ed927a9f72
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07361743B2

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