Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59326Generated: October 29, 2026

Cyclopropanecarbonyl chloride → Methyl 2-chloro-5-(cyclopropanecarboxamidomethyl)benzoate

https://huagongshe.com/reaction/59326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarbonyl chlorideHCID 77637—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 5-(aminomethyl)-2-chlorobenzoateHCID 66524841—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-chloro-5-(cyclopropanecarboxamidomethyl)benzoateHCID 89443034—

Reaction Steps

To a solution of methyl 5-(aminomethyl)-2-chlorobenzoate (15.0 g, 75 mmol) in dry THF (150 mL) was added DIPEA (15 mL) under nitrogen atmosphere. Cyclopropanecarbonyl chloride was added to the reaction mixture at 10° C. and (11.81 g, 113 mmol). The reaction mixture was stirred at RT for 5-6 h. The reaction mixture was quenched with ice water and extracted with ethyl acetate. The organic layer was washed with dilute HCl, followed with sodium bicarbonate solution and concentrated to afford 10.0 g of desired product. 1H NMR (300 MHz, DMSO d6): δ 0.69 (m, 4H), 1.59 (m, 1H), 3.86 (s, 3H), 4.29 (d, J=6.0 Hz, 2H), 7.43 (d, J=6.6 Hz, 1H), 7.53 (d, J=8.4 Hz, 1H), 7.67 (s, 1H), 8.64 (br s, 1H); MS (m/z): 268.16 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09439890B2
Source datasetuspto-grants-2016_09
ORD IDord-a60cd1d3a9874fa787e00ca79b1cef7a
Source noteuspto-grants-2016_09