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p-Toluenesulfonate → HCID 68527750, 화합물

HRID 2221307
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HRID 2221307 반응식
[C:1]1([S:7]([C:10]2[CH:24]=[CH:23][C:13]([O:14][CH2:15][C@@H:16]3[CH2:20]CC(C)(C)[O:17]3)=[C:12]([Br:25])[CH:11]=2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C1(C)C=CC(S([O-])(=O)=[O:33])=CC=1>CC(C)=O.O>[C:1]1([S:7]([C:10]2[CH:24]=[CH:23][C:13]([O:14][CH2:15][C@H:16]([OH:17])[CH2:20][OH:33])=[C:12]([Br:25])[CH:11]=2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 85570p-ToluenesulfonateHCID 68525779HCID 68525779, 화합물

생성물 1

HCID 68527750HCID 68527750, 화합물

시약·촉매·용매 2

HCID 180Acetone용매HCID 962Water용매

실험 절차

A solution of 4-(S)-(4-benzenesulfonyl-2-bromo-phenoxymethyl)-2,2-dimethyl-[3,3]dioxolan (1.07 g, 0.0025 mol) and pyridinum toluene-4-sulfonate (0.38 g, 0.0015 mol) in acetone (20 mL) and water (5 mL) was heated under reflux for 12 hours. The solvent was removed under reduced pressure. The oily residue was dissolved in ethyl acetate (100 mL), washed with cold 10% aqueous hydrochloric acid, saturated sodium bicarbonate, dried (Na2SO4) and concentrated in vacuo. Recrystallization of the residue (diethyl ether-hexane) gave 3-(4-benzenesulfonyl-2-bromo-phenoxy)-propane 1-2-(R)-diol as white crystals. Mp. 104.6-105.9° C.

후처리

  1. temperatureunder reflux for 12 hours
  2. customThe solvent was removed under reduced pressure
  3. dissolutionThe oily residue was dissolved in ethyl acetate (100 mL)
  4. washwashed with cold 10% aqueous hydrochloric acid, saturated sodium bicarbonate
  5. dry with materialdried (Na2SO4)
  6. concentrationconcentrated in vacuo
  7. customRecrystallization of the residue (diethyl ether-hexane)

출처 및 근거

ORD 기록
ord-a207f1aad45843e7b2027ed71c85f764
출처 데이터셋
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07368567B2

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