Hydrochloric Acid → HCID 18521038, compound
Reaction equation
O.[OH-].[Li+].C[O:5][C:6]([C:8]1[CH:13]=[CH:12][C:11]([C:14]2[CH:19]=[CH:18][C:17]([O:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH3:38])=[CH:16][CH:15]=2)=[CH:10][CH:9]=1)=[O:7].Cl>O.C1COCC1>[CH2:21]([O:20][C:17]1[CH:16]=[CH:15][C:14]([C:11]2[CH:12]=[CH:13][C:8]([C:6]([OH:7])=[O:5])=[CH:9][CH:10]=2)=[CH:19][CH:18]=1)[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH3:38]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
Lithium hydroxide monohydrate (874 mg, 20.8 mmol) was added to a suspension of the ester 28a (2.00 g, 4.17 mmol), 50 ml water, and 200 ml THF. The mixture was refluxed for 48 hours and then was acidified with concentrated HCl. Water (150 ml) was added and the solution was cooled. The resulting tan precipitate was filtered and washed with water. The tan precipitate was dissolved in 100 ml hot THF and hexanes were added until the solution remained cloudy with stirring. After cooling, crystals were filtered to yield 1.4 g of a light yellow solid, and a second crop of crystals was isolated for a total yield of 1.67 g (86%). The product was used without further purification.
Workup
- temperatureThe mixture was refluxed for 48 hours
- temperaturethe solution was cooled
- filtrationThe resulting tan precipitate was filtered
- washwashed with water
- dissolutionThe tan precipitate was dissolved in 100 ml hot THF
- additionhexanes were added until the solution
- temperatureAfter cooling
- filtrationcrystals were filtered
Sources & evidence
- ORD record
- ord-302f8bf307eb4934a750bc5040171dba
- Source dataset
- uspto-grants-2003_05
- Patent number
- US06569504B1
Reaction notes
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