HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Sulfate → 3-Pentyl-3-phenylazetidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Sodium sulphate hydrate | HCID 45051631 | — |
| Reactant | Toluene-4-sulfonic acid 2-cyano-2-phenylheptyl ester | HCID 86659207 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Pentyl-3-phenylazetidine | HCID 66987886 | 101.2% |
Reaction Steps
To a solution containing 5.26 g (14.1 mmol) of toluene-4-sulfonic acid 2-cyano-2-phenylheptyl ester in 25 mL of THF under nitrogen are added cautiously 600 mg (15.5 mmol) of LiAlH4 powder. The reaction medium is stirred for 1 hour at room temperature and then treated with a sodium sulfate paste (hot water+Na2SO4). After stirring for 30 minutes at room temperature, the salts formed are filtered off and the filtrate is evaporated under reduced pressure. The residue is taken up in dichloromethane and washed with aqueous 1N sodium hydroxide solution. The organic phase is dried over sodium sulfate, filtered and evaporated under reduced pressure. 2.90 g of a colourless oil are obtained and used in the following step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877968B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-b953abbd11b24a76b0c4eccccfbf6066 |
| Source note | uspto-grants-2014_11 |