홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Sodium Iodide → Didecyl Ether

HRID 2298786
노트
인쇄 미리보기

반응식

HRID 2298786 반응식
[H-].[Na+].[Na+].[I-].[CH2:5]([OH:9])[CH2:6][CH2:7]O.[H][H].[CH2:12](Cl)[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21]>CN(C=O)C.O>[CH2:12]([O:9][CH2:5][CH2:6][CH2:7][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

HCID 5238Sodium IodideHCID 104421,3-PropanediolHCID 138481-ChlorodecaneHCID 24758Sodium hydrideHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 17152Didecyl Ether

시약·촉매·용매 2

HCID 962Water
용매
HCID 6228Dimethylformamide용매2회

실험 절차

To a mixture of NaH (2.6 g, 70 mmol) and anhydrous NaI (9.9 g, 70 mmol) in dry DMF (80 mL) under N2 was added dropwise a solution of 1,3-propanediol (4.75 mL, 70 mmol) in DMF (20 mL). The mixture was stirred until hydrogen evolution had ceased, decyl chloride (1.34 g, 7.6 mmol) was added and stirring was continued at 50° C. for 18 hours. Then, the reaction mixture was poured into H2O (300 mL) and extracted with diethyl ether (3×250 mL). The organic extracts were combined, washed with sat. NaCl (100 mL), dried (MgSO4) and evaporated to dryness. The residue was subjected to silica-gel column chromatography [eluent: ethyl acetate/hexane, 30/70, v/v] to furnish decyl ether Compound 17 as a colourless oil.

후처리

  1. extractionextracted with diethyl ether (3×250 mL)
  2. washwashed with sat. NaCl (100 mL)
  3. dry with materialdried (MgSO4)
  4. customevaporated to dryness

출처 및 근거

ORD 기록
ord-636c22d6e1c1429b88dbee534f3a1166
출처 데이터셋
uspto-grants-2002_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06495532B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트