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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091603Generated: November 1, 2026

Methyl 4-chloro-2-cyanobenzoate → HCID 70654885, compound

https://huagongshe.com/reaction/2091603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-chloro-2-cyanobenzoateHCID 10035560—
ReactantHCID 178461630HCID 178461630—
CatalystHCID 178460666HCID 178460666—
SolventDiethyl EtherHCID 3283—
ProductHCID 70654885HCID 7065488521%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 4-chloro-2-cyanobenzoate (2.0 g, 10.2 mmol) in Et2O (40 mL) was added Ti(OiPr)4 (3.43 ml, 11.7 mmol). After cooling to 0° C., a 3.0 M solution of EtMgBr in Et2O (6.8 ml, 20.4 mmol) was added slowly. The reaction was warmed to room temperature and stirred for 3 h. Upon completion, the reaction was quenched with 1.0 M HCl (20 mL) then filtered over celite. The layers were separated and the aqueous layer was washed with EtOAc (2×20 mL). The combined organics were dried over Na2SO4, then filtered and concentrated. The crude product was purified by flash chromatography over silica gel (2-5% MeOH/DCM eluent) to provide 6′-chlorospiro[cyclopropane-1,1′-isoindolin]-3′-one (400 mg, 21% yield) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.75 (br. s., 1H), 7.66 (d, J=8.5 Hz, 1H), 7.40-7.54 (m, 2H), 1.47 (dt, J=11.2, 2.8 Hz, 4H); MS m/z C10H8ClNO [M+1]+=194.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440652B2
Source datasetuspto-grants-2013_05
ORD IDord-2e7b2105776a48a69987180e1a1a9ed3
Source noteuspto-grants-2013_05