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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715391Generated: October 26, 2026

Hydrochloric Acid → 2-Chloro-N-cyclopropyl-5-(3-methoxy-propenyl)-benzamide

https://huagongshe.com/reaction/1715391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium CarbonateHCID 10340—
Reactant5-bromo-2-chloro-N-cyclopropylbenzamideHCID 4806983—
Reactant2-[(1E)-3-methoxyprop-1-en-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 16217443—
Solvent1-PropanolHCID 1031—
SolventDimethylformamideHCID 6228—
Product2-Chloro-N-cyclopropyl-5-(3-methoxy-propenyl)-benzamideHCID 6850751968%

Reaction Conditions

Temperature80 °C

Reaction Steps

5-Bromo-2-chloro-N-cyclopropyl-benzamide (19.3 g, 70.5 mmol) was dissolved in a mixture of DMF (350 mL) and 1-propanol (210 mL). Pd(OAc)2(PPh3)3 (2.64 g, 3.53 mmol) was added. (E)-2-(3-Methoxypropenyl)4,4,5,5-tetramethyl-1,3,2-dioxaborolane (15 mL, 70.5 mmol) was added through a syringe, and aq. 2M Na2CO3 (123 mL) was added. The mixture was stirred at 80° C. for 2 h, and allowed to cool to rt. Aq. 10% HCl was added carefully until a pH of 2 was reached. The solvents were partially removed under reduced pressure, and the residue was extracted with Et2O (3×). The combined org. extracts were washed with water and brine, dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (EtOAc/heptane 1:2→1:1→EtOAc) yielded the title compound (12.7 g, 68%). LC-MS: tR=0.82 min; ES+: 266.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799805B2
Source datasetuspto-grants-2010_09
ORD IDord-1a85f1401cbe4be7a7302f4adddee2b9
Source noteuspto-grants-2010_09