Carbon Dioxide → HCID 29003638, compound
Reaction equation
C([Li])CCC.Br[C:7]1[CH:12]=[CH:11][C:10]([O:13][C@H:14]([CH3:21])[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])=[C:9]([F:22])[CH:8]=1.[C:23](=[O:25])=[O:24].Cl>C1COCC1>[F:22][C:9]1[CH:8]=[C:7]([CH:12]=[CH:11][C:10]=1[O:13][C@H:14]([CH3:21])[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])[C:23]([OH:25])=[O:24]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -78 °C
Procedure
A solution of n-butyllithium (2.5 M, 17.2 ml, 0.043 mol) in hexanes was added, dropwise, to a cooled (−78° C.), stirred solution of compound 35 (10.00 g, 0.033 mol) in dry THF (100 ml) under a dry nitrogen atmosphere and left to stir for 20 min. The resultant solution was poured into a slush of solid carbon dioxide and dry THF. This was left overnight at room temperature and then acidified with dilute hydrochloric acid. The THF/water azeotrope was evaporated off in vacuo and the residue was dissolved in diethyl ether, washed with water and then extracted with 5% sodium hydroxide solution which was acidified with dilute hydrochloric acid. The product was extracted with diethyl ether and the ethereal solution was washed with water until acid-free, dried (MgSO4) and evaporated in vacuo to leave an off-white, semi-solid.
Workup
- waitleft
- waitThis was left overnight at room temperature
- customThe THF/water azeotrope was evaporated off in vacuo
- dissolutionthe residue was dissolved in diethyl ether
- washwashed with water
- extractionextracted with 5% sodium hydroxide solution which
- extractionThe product was extracted with diethyl ether
- washthe ethereal solution was washed with water until acid-free,
- dry with materialdried (MgSO4)
- customevaporated in vacuo
- customto leave an off-white, semi-solid
Sources & evidence
- ORD record
- ord-a743d0d146594bfaac4809554496763d
- Source dataset
- uspto-grants-2002_01
- Patent number
- US06337420B1
Reaction notes
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