Ethyl Acetate → HCID 10018093, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([C:8]2[C:12]([CH3:13])=[C:11]([C:14]3[CH:19]=[CH:18][C:17]([OH:20])=[CH:16][CH:15]=3)[S:10][C:9]=2[CH:21]=[N:22]O)[CH:5]=[CH:6][CH:7]=1.Cl.[NH+]1C=CC=CC=1.C(OCC)(=O)C>C(OCC)(=O)C.CCCCCC>[OH:1][C:2]1[CH:3]=[C:4]([C:8]2[C:12]([CH3:13])=[C:11]([C:14]3[CH:19]=[CH:18][C:17]([OH:20])=[CH:16][CH:15]=3)[S:10][C:9]=2[C:21]#[N:22])[CH:5]=[CH:6][CH:7]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 200 °C
Procedure
A mixture of 3-(3-hydroxyphenyl)-5-(4-hydroxyphenyl)-4-methylthiophene-2-carbaldehyde oxime (0.76 g, 2.3 mmol) and pyridinium hydrochloride (2.7 g, 23 mmol) was heated at 195-205° C. in a 200 mL round bottom flask fitted with a 250 mL bump trap. After 2 h, the reaction mixture was cooled to 23° C. and taken up in a minimum of ethyl acetate (100 mL). The organic phase was washed with water (2×50 mL), saturated aqueous NaHCO3 (50 mL) and brine (50 mL), dried (Na2SO4) and concentrated in vacuo to give the crude product as a brown solid (0.61 g) which was pre-adsorbed on silica gel (2 g). Flash chromatography (10 g silica gradient 20%-30%-40% ethyl acetate-hexane) gave the title compound (0.37 g, 52%, m.p. 220-22° C.) as a pale orange solid after recrystallization from hot ethyl acetate-hexane.
Workup
- customfitted with a 250 mL bump trap
- temperaturethe reaction mixture was cooled to 23° C.
- washThe organic phase was washed with water (2×50 mL), saturated aqueous NaHCO3 (50 mL) and brine (50 mL)
- dry with materialdried (Na2SO4)
- concentrationconcentrated in vacuo
- customto give the crude product as a brown solid (0.61 g) which
Sources & evidence
- ORD record
- ord-09c72a4aba57446e9d52f55935fb5b20
- Source dataset
- uspto-grants-2004_12
- Patent number
- US06835745B2
Reaction notes
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