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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392972Generated: October 29, 2026

Dichloromethane → HCID 54537938, compound

https://huagongshe.com/reaction/2392972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantLactonitrileHCID 6572—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 53824756HCID 53824756—
SolventPyridineHCID 1049—
SolventChloranyl--pyridine (1/1)HCID 15387381—
ProductHCID 54537938HCID 54537938—

Reaction Steps

A flask containing 5 mL of CH2Cl2 under a layer of argon was cooled in an ice bath. Pyridine (0.5 mL) was added followed by slow addition of POCl3 (465 mg) and stirring continued for 15 min. A solution of the alkene (360 mg) from step (g) in 0.5 mL of 1:1 CH2 Cl2 /pyridine was added dropwise. The ice bath was removed and the solution stirred for 135 min. To this solution was added 1.0 mL of pyridine and 0.69 mL of 2-cyanoethanol. The reaction mixture was stirred for 4 hours resulting in formation of a white precipitate. TLC showed formation of two materials. Adding an additional 200 μL of cyanoethanol caused the precipitate to dissolve but stirring over night was without effect. The solution was evaporated to dryness and the crude product purified chromatographically. 1H NMR (CDCl3) δ1.79-1.98 (m, 14H), 2.41 (t,2H), 2.61 (br s,1H), 2.80 (m,4H), 3.23 (br s,1H), 3.41 (t,2H), 3.65 (s,3H), 4.32-4.48 (m,4H), 7.15-7.37 (m,4H). ##STR28##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05804103
Source datasetuspto-grants-1998_09
ORD IDord-33a1714413554829be4222b30b904aa0
Source noteuspto-grants-1998_09