O-Cresol → HCID 89668322, compound

HRID 1482261Notes

Reaction equation

HRID 1482261 reaction equation
Cl[C:2]([S:4]Cl)=[O:3].[C:6]1([CH3:13])[C:11]([OH:12])=[CH:10][CH:9]=[CH:8][CH:7]=1.C(N(CCCC)CCCC)CCC.[Cl-].[Al+3].[Cl-].[Cl-]>ClC(Cl)C.O>[CH3:13][C:6]1[C:11]2[O:12][C:2](=[O:3])[S:4][C:10]=2[CH:9]=[CH:8][CH:7]=1

Participants

7

Procedure

Chlorocarbonylsulfenyl chloride (30.5 mmol, 2.58 ml) was added to a solution of o-cresol (Compound 101) (27.7 mmol, 3.00 g) and tributylamine (30.5 mmol, 7.35 ml) in dichloroethane (48 mL) at 0° C., and the mixture was stirred at room temperature for 2 hours. Aluminum chloride (66.6 mmol, 8.88 g) was then added to the reaction mixture at 0° C., and the mixture was stirred at room temperature overnight. Water (10 ml) was then added to the reaction mixture at 0° C., after which the mixture was extracted with ethyl acetate and the organic layer was washed with water. The organic extract was then dried over sodium sulfate. Following concentration under reduced pressure, the resulting residue was purified by reverse-phase silica gel column chromatography (0.1% aqueous formic acid solution/0.1% formic acid-acetonitrile solution=100/0→30/70) to afford 7-methylbenzo[d][1,3]oxathiol-2-one (Compound 102) (2.46 g, 53%).

Workup

  1. stirringthe mixture was stirred at room temperature overnight
  2. extractionafter which the mixture was extracted with ethyl acetate
  3. washthe organic layer was washed with water
  4. extractionThe organic extract
  5. dry with materialwas then dried over sodium sulfate
  6. concentrationconcentration under reduced pressure
  7. customthe resulting residue was purified by reverse-phase silica gel column chromatography (0.1% aqueous formic acid solution/0.1% formic acid-acetonitrile solution=100/0→30/70)

Sources & evidence

ORD record
ord-09d9b39454154cc289cd58c283e68f07
Source dataset
uspto-grants-2016_08
Patent number
US09409952B2

Reaction notes

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