Aluminum(III) Chloride → 4,4-Dimethyl-6-bromo-2-oxo-thiochroman

HRID 52372Notes

Reaction equation

HRID 52372 reaction equation
[Cl-].[Al+3].[Cl-].[Cl-].[CH3:5][C:6]([CH3:18])=[CH:7][C:8]([S:10][C:11]1[CH:16]=[CH:15][C:14]([Br:17])=[CH:13][CH:12]=1)=[O:9]>C(Cl)Cl.[Cl-].[Na+].O>[CH3:5][C:6]1([CH3:18])[C:12]2[C:11](=[CH:16][CH:15]=[C:14]([Br:17])[CH:13]=2)[S:10][C:8](=[O:9])[CH2:7]1

Participants

5

Procedure

To a stirred, ice-cooled suspension of 15.9 g (119 mmol) of aluminum chloride in 140 ml of methylene chloride was added under nitrogen a solution of 21.64 g (79.9 mmol) of S-(4-bromophenyl) 3,3-dimethyl-thioacrylate (Compound 30) in 100 ml of methylene chloride. The mixture was then stirred at room temperature for 72 h and then poured into 250 g of an ice and brine mixture. The mixture was extracted with methylene chloride and the combined organic extracts were washed with saturated NaCl solution and then dried (MgSO4). The solvent was removed in vacuo and the residue recrystaliized from hexanes to give the title compound as white crystals. PMR (CDCl3): & 1.40 (6H, s), 2.67 (2H, s), 7.31-7.40 (3H, m). MS exact mass, m/e 269.9714 (calcd. for C11H11SOBr, 269.9714).

Workup

  1. temperatureTo a stirred, ice-cooled
  2. extractionThe mixture was extracted with methylene chloride
  3. washthe combined organic extracts were washed with saturated NaCl solution
  4. dry with materialdried (MgSO4)
  5. customThe solvent was removed in vacuo

Sources & evidence

ORD record
ord-9a99d840785e42639052de05c2271cec
Source dataset
uspto-grants-1997_04
Patent number
US05616597

Reaction notes

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