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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888090Generated: November 1, 2026

Dichloromethane → HCID 67119786, compound

https://huagongshe.com/reaction/1888090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantAcetone cardiceHCID 18522661—
ReactantHCID 25167670HCID 25167670—
ProductHCID 67119786HCID 6711978637.2%

Reaction Conditions

Temperature-75 °C

Reaction Steps

N-(benzo[d][1,3]dioxol-5-ylmethyl)-4-benzoylmethyl-4-piperidinol (III-13) is firstly prepared according to the method of synthesis and post-treatment in Example 13. 1.41 g (4.0 mmol) of N-(benzo[d][1,3]dioxol-5-ylmethyl)-4-benzoylmethyl-4-piperidinol is dissolved into 20 ml of anhydrous dichloromethane and cooled with dry ice-acetone with temperature controlled at below <−70° C. The reaction solution is added a dichloromethane solution (8 mol, 25 ml) of DAST under protection of nitrogen gas. After completion of addition, the temperature is maintained at −75° C. and reacting for 1 hour, and the temperature is raised slowly and maintained at −10° C. and reacting for 2 hours. Then operating according to the post-treatment method in General Method six obtains 0.61 g of a white crystal, with yield of 37.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501778B2
Source datasetuspto-grants-2013_08
ORD IDord-0ac90bb2c0714fd08fb85240db3a20b4
Source noteuspto-grants-2013_08