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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634699Generated: October 31, 2026

Dimethylformamide → HCID 18678921, compound

https://huagongshe.com/reaction/1634699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzhydrylamineHCID 7036—
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantEthyl AcrylateHCID 8821—
ReactantHCID 18678940HCID 18678940—
SolventEthanolHCID 702—
SolventPyridineHCID 1049—
ProductHCID 18678921HCID 1867892123%

Reaction Conditions

Temperature70 °C

Reaction Steps

Ethyl acrylate (1.05 g; 10.0 mmol) and diphenylmethyamine (1.83 g; 10.0 mmol) were dissolved in absolute ethanol (25 mL) and stirred overnight at 70° C. The solution was evaporated and crude ethyl 3-(diphenylmethylamino)propionate (2.85 g; 10.0 mmol) was dissolved in DMF (50 mL). 4-Methoxybenzenesulfonyl chloride (2.30 g; 11.0 mmol) and pyridine (10 mL) were added and the mixture stirred overnight at 70° C. The dark reaction was washed with 1 N HCl (2×100 mL). The combined extracts were washed with saturated aqueous NaCl (100 mL), dried over MgSO4, filtered, and evaporated to an oil. The black residue was eluted through a filter pad of silica gel using a hexanes/ethyl acetate step gradient to remove polar material. Preparative HPLC purification, eluting with a mixture of ethyl acetate/hexanes (35:65), gave 1.06 g (23%) of the title compound as a pale yellow oil. 300 MHz 1H-NMR (CDCl3): δ 1.16 (t, 3H), 2.12 (m, 2H), 3.57 (m, 2H), 3.84 (s, 3H), 3.99 (q, 2H), 6.48 (s, 1H), 6.83 (d, 2H), 7.04 (m, 4H), 7.24 (m, 6H), 7.64 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506936B1
Source datasetuspto-grants-2003_01
ORD IDord-bbd7ca22e7dd4f52955dd5816b9e6b00
Source noteuspto-grants-2003_01