HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → Trans-2,3,5,6,7,8-hexahydro-8-hydroxy-7-(N-propylamino)naphtho[2,3-b]thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Trans-2,3,5,6,7,8-hexahydro-8-hydroxy-7-propionylaminonaphtho[2,3-b]thiophene | HCID 70200501 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Trans-2,3,5,6,7,8-hexahydro-8-hydroxy-7-(N-propylamino)naphtho[2,3-b]thiophene | HCID 70201460 | 97% |
Reaction Steps
In a 500 ml three-necked flask fitted with a magnetic stirrer and a nitrogen inlet, 2.3 g (61 mmol) of AILiH4 are suspended in 75 ml of dry tetrahydrofuran. 6.2 g (24.5 mmol) of the product obtained in Step 2 dissolved in 97 ml of dry tetrahydrofuran are slowly added at room temperature. After 18 hours' stirring at room temperature, the reaction is stopped by the addition of 1.6 ml of water, 1.3 ml of 20 % NaOH in water and finally 5.8 ml of water in succession. The reaction mixture is stirred for 0.5 hour at room temperature and then filtered. The precipitate is washed copiously with tetrahydrofuran and the flitrate is concentrated in vacuo to yield 1.37 g of the expected product in the form of a meringue, Yield: 97 %.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05733908 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-04b5894104d743daa3447f348afad5c1 |
| Source note | uspto-grants-1998_03 |