Sodium Hydroxide → HCID 23530588, compound
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
Reactant 2
Product 1
Reagents, catalysts & solvents 2
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
- temperatureto cool
- washthe aqueous phase washed with DCM (50 mL)
- additionThe aqueous phase was treated with aqueous sodium bisulphite solution (10%, 20 mL)
- extractionThe resulting mixture was extracted with DCM (3×50 mL)
- dry with materialThe combined organic solutions were dried over sodium sulphate
- filtrationfiltered
- customevaporated
- customto give a yellow oil
- customPurification
- additionThe fractions containing product
- customevaporated
- 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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