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

HRID 1656055ノート

反応式

HRID 1656055 の反応式
[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]

参加物

6

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-6d978e2d64d849fdb074a8eecccb4ff5
出典データセット
uspto-grants-1993_10
特許番号
US05252601

反応ノート

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