Hydrochloric Acid → HCID 22316969, compound
Reaction equation
[CH2:1]([Li])CCC.Br[C:7]1[CH:11]=[CH:10][S:9][CH:8]=1.[B:12]([O:21]C(C)C)(OC(C)C)[O:13]C(C)C.Cl>C1COCC1>[CH:8]1[S:9][CH:10]=[CH:11][C:7]=1[CH2:1][B:12]([OH:21])[OH:13]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -78 °C
Procedure
n-Butyllithium (2.5 M solution in hexane, 20 ml, 50 mmol) was added dropwise to a solution of 3-bromothiophene (8.15 g, 50 mmol) in THF (20 ml) at -78° C. under an argon atmosphere. The resulting solution was stirred at -78° C. for 45 min, and then added to a solution of triisopropyl borate (9.4 g, 50 mmol) in THF at -78° C. over 30 min through a steel cannula. The resulting reaction mixture was stirred at room temperature for 12 h and was decomposed by the addition of 100 ml 1N HCl. The aqueous layer was extracted with ether (2×100 ml) and the combined organic layers was extracted with 1 M NaOH (3×30 ml), the aqueous extract was acidified with concentrated HCl to pH 2 and extracted with ether (3×50 ml). The combined ether extract was washed once with water, dried over MgSO4 and filtered. Removal of the solvent gave 3-thenylboronic acid as a solid (5.2 g, 80% yield).
Workup
- customThe resulting reaction mixture
- stirringwas stirred at room temperature for 12 h
- extractionThe aqueous layer was extracted with ether (2×100 ml)
- extractionthe combined organic layers was extracted with 1 M NaOH (3×30 ml)
- extractionthe aqueous extract
- extractionextracted with ether (3×50 ml)
- extractionThe combined ether extract
- washwas washed once with water
- dry with materialdried over MgSO4
- filtrationfiltered
- customRemoval of the solvent
Sources & evidence
- ORD record
- ord-9f0dd6e90745437fa6201283303af40e
- Source dataset
- uspto-grants-1999_10
- Patent number
- US05962490
Reaction notes
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