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

Sodium Thiosulfate → 9-Hydroxy-5,9-dimethyl-decanal

HRID 493069
노트
인쇄 미리보기

반응식

HRID 493069 반응식
[CH3:1][C@@H:2]([CH2:8][CH2:9][CH2:10][C:11]([CH3:14])([OH:13])[CH3:12])[CH2:3][CH2:4][CH2:5][CH2:6][OH:7].CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.S([O-])([O-])(=O)=S.[Na+].[Na+].C([O-])(O)=O.[Na+]>C(Cl)Cl>[OH:13][C:11]([CH3:12])([CH3:14])[CH2:10][CH2:9][CH2:8][CH:2]([CH3:1])[CH2:3][CH2:4][CH2:5][CH:6]=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 24477Sodium ThiosulfateHCID 159087TriacetoxyperiodinaneHCID 516892Sodium BicarbonateHCID 15859989(R)-5,9-dimethyl-decane-1,9-diol

생성물 1

HCID 218389029-Hydroxy-5,9-dimethyl-decanal수율 68.6%

시약·촉매·용매 1

HCID 6344Dichloromethane
용매

실험 절차

To a stirred solution of diol 14 (25 mg, 0.12 mmol) in anhydrous CH2Cl2 (3.5 mL) was added Dess-Martin reagent (73 mg, 0.15 mmol) at room temperature. The reaction was stirred at room temperature for 1.5 hours. Then, an aqueous solution of sodium thiosulfate (6 mL) and saturated NaHCO3 (6 mL) were added. The reaction was extracted with CH2Cl2, solvents were removed under reduced pressure, and the crude oil was purified on silica Sep-Pak using hexane/EtOAc (7:3) as an eluent to give an oily aldehyde 15 (16.5 mg, 67%).

후처리

  1. extractionThe reaction was extracted with CH2Cl2, solvents
  2. customwere removed under reduced pressure
  3. customthe crude oil was purified on silica Sep-Pak

출처 및 근거

ORD 기록
ord-04b62b99c1f547bda46c3ce7d97e2253
출처 데이터셋
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07534777B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트