Hydrochloric Acid → 2-(N,N-dimethylsulphamoyl)benzeneboronic acid
Reaction equation
[CH3:1][N:2]([CH3:12])[S:3]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)(=[O:5])=[O:4].[Li]CCCC.CCCCCC.[B:24](OC(C)C)([O:29]C(C)C)[O:25]C(C)C.Cl>CCOCC>[CH3:1][N:2]([CH3:12])[S:3]([C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][C:11]=1[B:24]([OH:29])[OH:25])(=[O:4])=[O:5]Participants
Conditions
- Temperature
- -70 °C
Procedure
A solution of N,N-dimethylbenzenesulfonamide (9.25 g; 50 mmol) in dry Et2O (150 ml) under N2 was cooled to −70° C. and added a solution of 2.5 M n-BuLi in hexane (24 ml; 60 mmol) such that the reaction temperature was kept below −60° C. The cooling bath was removed and the reaction mixture allowed to slowly warm up to +20° C. The reaction mixture was re-cooled to −70° C. and B(Oi-Pr)3 (16.1 ml; 70 mmol) was added. The reaction mixture was left cold and allowed to warm up over night, 1 M HCl (100 ml) was added and stirring was continued at rt. for 1 h. The reaction mixture was then extracted with Et2O (2×50 ml) and the combined organic fractions extracted with 1 M NaOH (4×50 ml). The combined aqueous fractions were neutralized with 1 M HCl and extracted with Et2O (4×100 ml). The combined organic fractions were dried (Na2SO4) and evaporated to dryness, washed with Et2O/hexane to give 3.4 g (30%) product.
Workup
- customwas kept below −60° C
- customThe cooling bath was removed
- temperatureto slowly warm up to +20° C
- waitThe reaction mixture was left cold
- temperatureto warm up over night
- customwas continued at rt
- extractionThe reaction mixture was then extracted with Et2O (2×50 ml)
- extractionthe combined organic fractions extracted with 1 M NaOH (4×50 ml)
- extractionextracted with Et2O (4×100 ml)
- dry with materialThe combined organic fractions were dried (Na2SO4)
- customevaporated to dryness
- washwashed with Et2O/hexane
Sources & evidence
- ORD record
- ord-8ea65a99d7f74ecb9f407694ee52ef25
- Source dataset
- uspto-grants-2007_06
- Patent number
- US07235548B2
Reaction notes
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