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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421611Generated: November 2, 2026

Dichloromethane → HCID 67214322, compound

https://huagongshe.com/reaction/2421611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPiperidineHCID 8082—
ReactantPhenylacetyleneHCID 10821—
Reactant3-iodo-N-propylbenzamideHCID 3409108—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
ProductHCID 67214322HCID 67214322—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of N-n-propyl-3-iodobenzamide, phenylacetylene (1.5 eq.) and Pd(PPh3)2Cl2 (5 mol %) in piperidine (3 eq.) was heated at 70° C. for 30 minutes in a sealed tube. The solidified residue was dissolved with CH2Cl2 and water and poured onto HCl 2N. The acidic phase was extracted three times with CH2Cl2. The combined organic layers were washed once with HC 2N, twice with saturated NaHCO3, once with water and once with brine. The organic layer was then dried over MgSO4 and concentrated. The resulting residue was purified using SiO2 with CH2Cl2/petroleum ether 80:20 to CH2Cl2 100% to give N-n-propyl-3-phenylethynyl-benzamide as a yellow solid (Quantitative yield). NMR 1H (ppm, CDCl3): 7.88 (s, 1H), 7.74-7.68 (m, 1H), 7.63-7.60 (m, 1H), 7.53-7.50 (m, 2H), 7.42-7.33 (m, 4H), 6.22 (br. s., 1H), 3.44-3.38 (m, 2H), 1.64 (sext., J3=7.3 Hz, 2H), 0.98 (t, J3=7.3 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956216B2
Source datasetuspto-grants-2011_06
ORD IDord-2fd1b09e7ed541d8a3186f141927306f
Source noteuspto-grants-2011_06