Hydrogen Sulfide → 2-Carboxy-2-[(acetylthio)methyl]-1,2,3,4-tetrahydronaphthalene

HRID 1656055

반응식

HRID 1656055 반응식
[C:1]([C:4]1([CH2:14][S:15][C:16]([CH3:19])(C)C)[CH2:13][CH2:12][C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH2:5]1)([OH:3])=[O:2].S.C(OC(=O)C)(=[O:23])C>FC(F)(F)C(O)=O.C(OCC)C>[C:1]([C:4]1([CH2:14][S:15][C:16](=[O:23])[CH3:19])[CH2:13][CH2:12][C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH2:5]1)([OH:3])=[O:2]

참가 물질

6

실험 절차

Dissolve 2-carboxy-2-(t-butyl)thiomethyl-1,2,3,4-tetrahydronaphthalene (5.36 g, 20.0 mmol) in trifluoroacetic acid (40 mL) and add mercuric acetate (6.36 g, 20.0 mmol). Stir at ambient temperature under an atmosphere of argon for 4.5 hours, then treat with gaseous hydrogen sulfide. Remove the resulting black solid by filtration and dilute the filtrate to 100 mL with methylene chloride. Wash with water, then with brine and dry (MgSO4). Evaporate the solvent in vacuo to a residue. Mix the residue with sulfuric acid (0.3 mL of 10% solution in acetic acid) and add acetic anhydride (2.04 g, 20.0 mmol). Stir the mixture for 2 hours under an atmosphere of argon at ambient temperature, then dilute with 100 mL ethyl ether. Wash with water, brine then dry (MgSO4). Concentrate the filtrate in vacuo to give the title compound.

후처리

  1. customRemove the resulting black solid
  2. filtrationby filtration
  3. additiondilute the filtrate to 100 mL with methylene chloride
  4. washWash with water
  5. dry with materialwith brine and dry (MgSO4)
  6. customEvaporate the solvent in vacuo to a residue
  7. additionMix the residue with sulfuric acid (0.3 mL of 10% solution in acetic acid)
  8. stirringStir the mixture for 2 hours under an atmosphere of argon at ambient temperature
  9. washWash with water, brine
  10. dry with materialthen dry (MgSO4)
  11. concentrationConcentrate the filtrate in vacuo

출처 및 근거

ORD 기록
ord-6d978e2d64d849fdb074a8eecccb4ff5
출처 데이터셋
uspto-grants-1993_10
특허 번호
US05252601

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