HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 67119893, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 25167673 | HCID 25167673 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67119893 | HCID 67119893 | 39.9% |
Reaction Steps
N-(1-(4-methoxyphenyl)ethyl)-4-benzoylmethyl-4-piperidinol (III-19) is firstly prepared according to the method of synthesis and post-treatment in Example 19. 1.41 g (4.0 mmol) of N-(1-(4-methoxyphenyl)ethyl)-4-benzoylmethyl-4-piperidinol is dissolved into 20 ml of anhydrous dichloromethane and cooled in an ice-water bath with temperature controlled at below 0° C. The reaction solution is added dropwise a dichloromethane solution (8 mol, 25 ml) of SOCl2. After completion of addition, the temperature is raised slowly to room temperature and reacting for 1 hour. Then operating according to the post-treatment method in General Method seven obtains 0.68 g of white crystal, with yield of 39.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08501778B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-fb3abb78313e47d2b137faa1d6416db1 |
| Source note | uspto-grants-2013_08 |