Réaction #6638

ord-fd81178d17144eccb85427ba5786701d

Équation de réaction

CC1(C)CC(C)(C)c2cc(C#C[Si](C)(C)C)ccc2S1
Compound 73
CC1(C)CC(C)(C)c2cc(C#C[Si](C)(C)C)ccc2S1
2,2,4,4-Tetramethyl-6-trimethylsilylethynyl-thiochroman
[K+].[OH-]
KOH
C#Cc1ccc2c(c1)C(C)(C)CC(C)(C)S2
title compound
C#Cc1ccc2c(c1)C(C)(C)CC(C)(C)S2
2,2,4,4-Tetramethyl-6-ethynylthiochroman

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe isopropanol was then removed under vacuum
  2. 2
    ExtractionThe residue was extracted with ether
  3. 3
    Lavagethe combined ether extracts were washed successively with water and saturated NaCl solution
  4. 4
    Séchagedried (MgSO4) The solvent
  5. 5
    Autrewas removed in vacuo

Mode opératoire

To a solution of 527.6 mg (1.75 mmol) of 2,2,4,4-tetramethyl-6-trimethylsilyl-ethynylthiochroman (Compound 73) in 4 ml of isopropanol was added, under argon, 4 ml of 1N KOH solution. The reaction mixture was stirred at room temperature for 20 h and the isopropanol was then removed under vacuum. The residue was extracted with ether and the combined ether extracts were washed successively with water and saturated NaCl solution and then dried (MgSO4) The solvent was removed in vacuo to give the title compound as a yellow oil. PMR (CDCl3): δ 1.34 (6H, s), 1.37 (6H, s), 1.91 (2H, s), 2.99 (1H, s), 7.17 (1H, dd, J~8.1 Hz, 1.8 Hz), 7.26 (1H, d, J~1.8 Hz), 7.30 (1H, d, J~8.1 Hz). MS exact mass, m/e 230.1122 (calcd. for C15H18S, 230.1129)

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05248777uspto-grants-1993_09