Boron tribromide → HCID 13091179, compound
Reaction equation
B(Br)(Br)Br.C[O:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:13]1[C:14](=[O:24])[CH:15]=[C:16]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[O:17][CH:18]=1>C(Cl)Cl.O>[OH:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:13]1[C:14](=[O:24])[CH:15]=[C:16]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[O:17][CH:18]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Boron tribromide (3.0 ml) was added dropwise to a stirred solution of ethyl 5-(2-methoxyphenyl)-4-oxo-4H-pyran-2-carboxylate (3.2 g) in methylene chloride (100 ml) at 5°-10° C. The mixture was stirred for 2 hours at room temperature, then cooled to 5° C. and carefully diluted with water (50 ml). The solid title product was recrystallised from ethanol (mp 187°-189° C.).
Workup
- temperaturecooled to 5° C.
- customThe solid title product was recrystallised from ethanol (mp 187°-189° C.)
Sources & evidence
- ORD record
- ord-47cc60e7f85c408197a83e325fcdc6fd
- Source dataset
- uspto-grants-1982_12
- Patent number
- US04364956
Reaction notes
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