HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 15860332, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-(Methylsulfonyl)benzaldehyde | HCID 220376 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 5-fluoro-2-methyl-1H-3-indenyl-(2-hydroxy) ethane | HCID 13933293 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15860332 | HCID 15860332 | — |
Reaction Steps
5-Fluoro-2-methyl-1H-3-indenyl-(2-hydroxy) ethane (15 g, 0.072 mol), p-methylsulfonylbenzaldehyde (14.0 g, 0.091 mol) and sodium methoxide (13.0 g, 0.24 mol) are heated in methanol (200 ml) at 60° C. under nitrogen with stirring for 6 hours. The reaction mixture is poured onto ice-water (750 g), and is acidified with 2.5N hydrochloric acid. The collected solid is triturated with a little ether to produce (Z)-5-fluoro-2-methyl-1-(p-methylsulfonylbenzylidene)-1H-3-indenyl-(2-hydroxy) ethane. Recrystallization of the crude reaction product results in the separation of the mixture of geometrical isomers (Z/E) and gives the title compound (R1 =5-fluror, R2 =CH3, R3 =H, R4 =CH2OH, n=1, R5 =CH3SO2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06025394 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-0c443b68506842a49d541f85a1283d38 |
| Source note | uspto-grants-2000_02 |