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

Hexane → HCID 22033402, 화합물

HRID 1792332
노트
인쇄 미리보기

반응식

HRID 1792332 반응식
[CH3:1][O:2][CH:3]([O:19][CH3:20])[CH2:4][CH2:5][CH2:6][CH2:7][S:8][CH2:9][CH2:10][CH2:11][C:12]([F:18])([F:17])[C:13]([F:16])([F:15])[F:14].I([O-])(=O)(=O)=[O:22].[Na+].CCCCCC.C(OCC)(=O)C>CO.O>[CH3:20][O:19][CH:3]([O:2][CH3:1])[CH2:4][CH2:5][CH2:6][CH2:7][S:8]([CH2:9][CH2:10][CH2:11][C:12]([F:17])([F:18])[C:13]([F:16])([F:14])[F:15])=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 8058HexaneHCID 8857Ethyl AcetateHCID 220330545,5-Dimethoxy-1-(4,4,5,5,5-pentafluoropentylthio)pentaneHCID 23667635Sodium periodate

생성물 1

HCID 22033402HCID 22033402, 화합물수율 76.6%

시약·촉매·용매 2

HCID 887Methanol용매2회
HCID 962Water용매2회

실험 절차

To a solution of 5,5-dimethoxy-1-(4,4,5,5,5-pentafluoropentylthio)pentane (460 mg, 1.4 mmol) in methanol (10 mg) were added sodium periodate (420 mg, 2.0 mmol) dissolved in water (8 ml) and methanol (5 ml), and the resulting mixture was stirred at room temperature for 2 hours. After the reaction was completed, the reaction solution was poured into water and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give a crude product. This crude product thus obtained was subjected to silica gel column chromatography (n-hexane:ethyl acetate=2:1) to give 5,5-dimethoxy-1-(4,4,5,5,5-pentafluoropentylsulfinyl)pentane (365 mg, yield 76%).

후처리

  1. extractionextracted with ethyl acetate
  2. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  3. concentrationconcentrated under reduced pressure
  4. customto give a crude product
  5. customThis crude product thus obtained

출처 및 근거

ORD 기록
ord-e4a8560b4fb846be894ecde8d8827abe
출처 데이터셋
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07074819B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트