Sodium Hydroxide → HCID 23530588, compound

HRID 1689388Notes

Reaction equation

HRID 1689388 reaction equation
[CH:1]([C:4]1[CH:5]=[C:6]([C:9](=[O:11])C)[S:7][CH:8]=1)([CH3:3])[CH3:2].[OH-:12].[Na+]>O1CCOCC1.Cl[O-].[Na+]>[CH:1]([C:4]1[CH:5]=[C:6]([C:9]([OH:11])=[O:12])[S:7][CH:8]=1)([CH3:2])[CH3:3]

Participants

5

Conditions

Temperature
75 °C

Procedure

A solution of 1-(4-isopropylthiophen-2-yl)ethanone (example 74, step a) (1 g) in 1,4-dioxane (10 mL) was cautiously added to a solution of sodium hydroxide (1.19 g) in aqueous sodium hypochlorite (8%, 50 mL) at 60° C. The resulting mixture was heated to 75° C. and stirred for 1 h. The reaction was allowed to cool and the aqueous phase washed with DCM (50 mL). The aqueous phase was treated with aqueous sodium bisulphite solution (10%, 20 mL) and carefully acidified with concentrated hydrochloric acid. The resulting mixture was extracted with DCM (3×50 mL). The combined organic solutions were dried over sodium sulphate, filtered and evaporated to give a yellow oil. Purification was by preparative HPLC (Sunfire™, Gradient: 5-95% acetonitrile in 0.2% aqueous TFA). The fractions containing product were combined, evaporated and dried under high vacuum to give the subtitled compound as a white solid. Yield 0.5 g.

Workup

  1. temperatureto cool
  2. washthe aqueous phase washed with DCM (50 mL)
  3. additionThe aqueous phase was treated with aqueous sodium bisulphite solution (10%, 20 mL)
  4. extractionThe resulting mixture was extracted with DCM (3×50 mL)
  5. dry with materialThe combined organic solutions were dried over sodium sulphate
  6. filtrationfiltered
  7. customevaporated
  8. customto give a yellow oil
  9. customPurification
  10. additionThe fractions containing product
  11. customevaporated
  12. customdried under high vacuum

Sources & evidence

ORD record
ord-1ac2306da87e478682bfadb97c76e7a0
Source dataset
uspto-grants-2012_04
Patent number
US08148373B2

Reaction notes

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