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Sodium Cyanide → 13-Hydroxyoctadecanenitrile

HRID 2204028
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HRID 2204028 반응식
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH:13]([OH:19])[CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].[C-:20]#[N:21].[Na+]>CN(C=O)C.C(OCC)C>[OH:19][CH:13]([CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][C:20]#[N:21]
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참가 물질

5

반응물 2

HCID 8929Sodium CyanideHCID 8669164217-Bromoheptadecan-6-ol

생성물 1

HCID 8669164313-Hydroxyoctadecanenitrile수율 92%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 6228Dimethylformamide용매

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온도
90 °C

실험 절차

To 17-bromoheptadecan-6-ol (1.0 g, 2.98 mmol) in dry DMF, was added NaCN (175 mg, 3.58 mmol) and the resulting reaction mixture heated at 90° C. for 16 hours. After cooling to room temperature, the mixture was diluted with diethyl ether (100 ml), the organic layer was washed with cold water (3×20 ml), brine solution, dried over MgSO4 and concentrated. The crude product was purified over a silica gel column (10% EtOAc in hexane) to give 13-hydroxyoctadecanenitrile as a colorless liquid (0.77 g, 92%).

후처리

  1. customthe resulting reaction mixture
  2. temperatureAfter cooling to room temperature
  3. washthe organic layer was washed with cold water (3×20 ml), brine solution
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated
  6. customThe crude product was purified over a silica gel column (10% EtOAc in hexane)

출처 및 근거

ORD 기록
ord-924e9ceda93b41f7a3a2ac89990b6621
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09365597B2

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