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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616478Generated: October 31, 2026

Methyl 5-chloro-2-ethynylbenzoate → Methyl 5-chloro-2-ethylbenzoate

https://huagongshe.com/reaction/1616478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-chloro-2-ethynylbenzoateHCID 86672667—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductMethyl 5-chloro-2-ethylbenzoateHCID 5938245393.9%

Reaction Steps

To a solution of methyl 5-chloro-2-ethynylbenzoate (5.34 g, 27.44 mmol) in Ethyl acetate (135 ml) was added Pd/C (10%) (50% water, 2.92 g, 1.37 mmol). The reaction mixture was stirred under a hydrogen atmosphere at room temperature for 3 hours. LCMS indicated the reaction had gone to completion and the mixture was filtered through Celite. The filter cake washed with EtOAc (50 ml) and the filtrate was concentrated under reduced pressure to give 5.12 g (93.9%) of methyl 5-chloro-2-ethylbenzoate as a brown oil which was suitable for use without any further purification. LC-MS 56%, 2.21 min (3 minute LC-MS method), m/z=198.9/200.9, 1H NMR (500 MHz, Chloroform-d) δ ppm 7.84 (d, J=2.3 Hz, 1H), 7.39 (dd, J=8.3, 2.3 Hz, 1H), 7.21 (d, J=8.3 Hz, 1H), 3.90 (s, 3H), 2.94 (q, J=7.5 Hz, 2H), 1.21 (t, J=7.5 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765732B2
Source datasetuspto-grants-2014_07
ORD IDord-382a2f8551c049628dc5eb281f0866e2
Source noteuspto-grants-2014_07