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

Acetone → Dihydro-2H-thiopyran-3(4H)-one-1,1-dioxide

HRID 247132
노트
인쇄 미리보기

반응식

HRID 247132 반응식
[CH3:1][C:2]([CH3:4])=[O:3].C[C:6]([CH3:8])=O.[OH:9][S:10](O)(=O)=[O:11].O=[Cr](=O)=O>C(O)(C)C>[S:10]1(=[O:11])(=[O:9])[CH2:6][CH2:8][CH2:4][C:2](=[O:3])[CH2:1]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 180AcetoneHCID 131709961Jones' reagent

생성물 1

HCID 11815935Dihydro-2H-thiopyran-3(4H)-one-1,1-dioxide

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

To a solution of tetrahydrothiopyran-3-o1-1,1-dioxide (7.5 g, 0.05 moles) and acetone (150 mL) was slowly added enough Jones reagent to maintain a brown color for at least 10 minutes without need for additional reagent. The excess reagent was reduced by addition of isopropanol (5 mL). The mixture was filtered through anhydrous magnesium sulfate and the chromium salts were washed 3× with acetone. The solvent was removed in vacuo to give a solid which was triturated with ethanol. The resulting crystals were isolated by filtration and rinsed 3× with diethyl ether. After drying, 5.0 g of product was obtained. H' NMR CDCl3 4.0 (singlet, 2H) 3.3 (triplet, 2H) 2.6 (triplet, 2H) 2.3 (multiplet, 2H).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperatureto maintain a brown color for at least 10 minutes without need for additional reagent
  2. filtrationThe mixture was filtered through anhydrous magnesium sulfate
  3. washthe chromium salts were washed 3× with acetone
  4. customThe solvent was removed in vacuo
  5. customto give a solid which
  6. customwas triturated with ethanol
  7. customThe resulting crystals were isolated by filtration
  8. washrinsed 3× with diethyl ether
  9. customAfter drying

출처 및 근거

ORD 기록
ord-30940996b59f43c28814748c6195402a
출처 데이터셋
uspto-grants-1987_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04705785

반응 노트

불러오는 중…