Réaction #1005977

ord-440eb576dccc4716a6192a3c366f500c

Équation de réaction

CC1(C)CC(=O)c2cc(C#C[Si](C)(C)C)ccc2S1
2,2-dimethyl-6-trimethylsilanylethynylthiochroman-4-one
O=C([O-])[O-].[K+].[K+]
K2CO3
C#Cc1ccc2c(c1)C(=O)CC(C)(C)S2
6-ethynyl-2,2-dimethylthiochroman-4-one
Rendement 99.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionextracted with Et2O
  2. 2
    LavageThe combined organic layers were washed with H2O and saturated aqueous NaCl
  3. 3
    Séchagedried over MgSO4
  4. 4
    AutreRemoval of the solvent under reduced pressure

Mode opératoire

A solution of 2,2-dimethyl-6-trimethylsilanylethynylthiochroman-4-one (110.0 mg, 0.38 mmol) and K2CO3 (40.0 mg, 0.29 mmol) in 10.0 mL MeOH was stirred overnight at room temperature. The solution was diluted with H2O and extracted with Et2O. The combined organic layers were washed with H2O and saturated aqueous NaCl and dried over MgSO4. Removal of the solvent under reduced pressure afforded 81 mg (99%) of the 6-ethynyl-2,2-dimethylthiochroman-4-one as an orange oil. 1H NMR (300 MHz, CDCl3) δ: 8.20 (1H, d, J=1.9 Hz), 7.46 (1H, dd, J=1.9, 8.1 Hz), 7.18 (1H, d, J=8.1 Hz), 3.08 (1H, s), 2.86 (2H, s), 1.46 (6H, s).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09271946B2uspto-grants-2016_03