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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888093Generated: November 1, 2026

Thionyl Chloride → HCID 67119893, compound

https://huagongshe.com/reaction/1888093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 25167673HCID 25167673—
SolventDichloromethaneHCID 6344—
ProductHCID 67119893HCID 6711989339.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501778B2
Source datasetuspto-grants-2013_08
ORD IDord-fb3abb78313e47d2b137faa1d6416db1
Source noteuspto-grants-2013_08