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Hexane → HCID 71307795, 화합물

HRID 532896
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HRID 532896 반응식
[CH3:1][C:2]1[O:6][CH:5]=[N:4][CH:3]=1.[Li]CCCC.CCCCCC.[Sn:18](Cl)([CH2:27][CH2:28][CH2:29][CH3:30])([CH2:23][CH2:24][CH2:25][CH3:26])[CH2:19][CH2:20][CH2:21][CH3:22]>CCOCC>[CH3:1][C:2]1[O:6][C:5]([Sn:18]([CH2:23][CH2:24][CH2:25][CH3:26])([CH2:27][CH2:28][CH2:29][CH3:30])[CH2:19][CH2:20][CH2:21][CH3:22])=[N:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8058HexaneHCID 15096Tributyltin ChlorideHCID 5284115-MethyloxazoleHCID 178418339Butyllithium

생성물 1

HCID 71307795HCID 71307795, 화합물수율 15.6%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

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온도
-78 °C

실험 절차

A solution of 5-methyloxazole (5.0 g, 60.2 mmol) in Et2O (100 mL) was cooled to −78° C. under N2 and treated with a 1.6 M solution of BuLi in hexane (41.4 mL, 66.2 mmol) dropwise. The mixture was stirred at −78° C. for 30 min and a solution of Bu3SnCl (16.31 mL, 60.2 mmol) in Et2O (50 mL) was then added dropwise. The mixture was stirred at −78° C. for another 30 min and then allowed to warm to RT. The reaction mixture was filtered on celite, and the filtrate concentrated in vacuo. Purification by distillation (0.1 Torr, 128-130° C.) afforded the title compound (3.5 g) as a yellow liquid. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 0.88 (m, 12 H) 1.14-1.22 (m, 6 H) 1.27-1.38 (m, 6 H) 1.52-1.61 (m, 6 H) 2.17-2.21 (m, 3 H) 7.49-7.54 (m, 1 H).

후처리

  1. stirringThe mixture was stirred at −78° C. for another 30 min
  2. temperatureto warm to RT
  3. filtrationThe reaction mixture was filtered on celite
  4. concentrationthe filtrate concentrated in vacuo
  5. customPurification
  6. distillationby distillation (0.1 Torr, 128-130° C.)

출처 및 근거

ORD 기록
ord-46bbe033228d47e5895f7fc9ce76a2f6
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08853203B2

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