Carbon Dioxide → HCID 63074857, compound
Reaction equation
C([Li])CCC.Br[C:7]1[CH:12]=[CH:11][C:10]([CH2:13][O:14][CH:15]2[CH2:18][CH2:17][CH2:16]2)=[C:9]([F:19])[CH:8]=1.[C:20](=[O:22])=[O:21]>C1COCC1.O>[CH:15]1([O:14][CH2:13][C:10]2[CH:11]=[CH:12][C:7]([C:20]([OH:22])=[O:21])=[CH:8][C:9]=2[F:19])[CH2:18][CH2:17][CH2:16]1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
n-Butyllithium (1.6 M in hexane; 7.0 ml) was added to a solution of 4-bromo-1-cyclobutoxymethyl-2-fluorobenzene (2.6 g) in THF (50 ml) at −78° C. After 15 minutes, dry ice (4.4 g) was added. After warming to room temperature, the mixture was diluted with water and extracted with ethyl acetate. The aqueous phase was acidified and again extracted with ethyl acetate. The organic phase was dried over magnesium sulfate, filtered and concentrated. The product with the molecular weight of 224.23 (C12H13FO3); MS (ESI): 225 (M+H+) was obtained in this way.
Workup
- extractionextracted with ethyl acetate
- extractionagain extracted with ethyl acetate
- dry with materialThe organic phase was dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customMS (ESI): 225 (M+H+) was obtained in this way
Sources & evidence
- ORD record
- ord-dc4d4851982e4bdcba5d5d899b68f63c
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08357686B2
Reaction notes
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