Sulfuric Acid → HCID 57097596, compound
Reaction equation
S(=O)(=O)(O)O.[OH:6][CH2:7][C:8]1[CH:13]=[CH:12][C:11]([CH:14]=[CH:15][C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([CH2:22][CH2:23][CH2:24][CH2:25][C:26]([CH3:35])([O:28]C3CCCCO3)[CH3:27])[CH:17]=2)=[CH:10][C:9]=1[CH2:36][OH:37]>C1COCC1.O>[OH:37][CH2:36][C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][C:16]2[CH:17]=[C:18]([CH2:22][CH2:23][CH2:24][CH2:25][C:26]([CH3:35])([OH:28])[CH3:27])[CH:19]=[CH:20][CH:21]=2)[CH:12]=[CH:13][C:8]=1[CH2:7][OH:6]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 40 °C
Procedure
0.09 ml of concentrated sulphuric acid are added to 44 mg (0.1 mmol) of [2-hydroxymethyl-5-(2-{3-[5-methyl-5-(tetrahydropyran-2-yloxy)hexyl]-phenyl}vinyl)phenyl]methanol in 1 ml of THF and 1 ml of water. The solution is heated at 40° C. for 48 hours. Water is added and the mixture is extracted with ether. The organic phase is dried over magnesium sulphate and concentrated. The product is triturated in an ether-hexane mixture and is then filtered and dried.
Workup
- extractionthe mixture is extracted with ether
- dry with materialThe organic phase is dried over magnesium sulphate
- concentrationconcentrated
- customThe product is triturated in an ether-hexane mixture
- filtrationis then filtered
- customdried
Sources & evidence
- ORD record
- ord-1f24f6974d464bfa92676d7f892af8bc
- Source dataset
- uspto-grants-2004_02
- Patent number
- US06689922B1
Reaction notes
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