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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132245Generated: October 26, 2026

Acetic Acid → Methyl 3-chloro-2-nitrobenzoate

https://huagongshe.com/reaction/132245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-Chloro-2-nitrobenzoic acidHCID 20902—
ReactantTrimethylsilyldiazomethaneHCID 167693—
SolventAcetonitrile methanolHCID 21959252—
ProductMethyl 3-chloro-2-nitrobenzoateHCID 1218712574.3%

Reaction Steps

To 3-chloro-2-nitrobenzoic acid (3.15 g, 15.6 mmol) in methanol/acetonitrile (20 mL/20 mL) was dropwise added TMSCHN2 (2N in hexanes, 11.7 mL, and 23.4 mmol) at 0° C. under N2 over 10 min until the yellow color persist. The mixture was continued stirring for 20 min, followed by dropwise addition of HOAc until the yellow color disappeared to kill excessive TMSCHN2. Partial of the solvent was removed on rotary vacuum, the product came out solution as a light yellow solid, which was filtered and washed with Et2O (2×2 mL) to afford the expected product as a white solid (2.5 g, 74% yield); 1H NMR (400 MHz, CDCl3) δ ppm 3.91 (s, 3 H), 7.51 (t, J=8.06 Hz, 1 H), 7.70 (dd, J=8.06, 1.26 Hz, 1 H), 7.97 (dd, J=7.81, 1.26 Hz, 1 H); Mass spec. 216.02 (MH+), Calc. for C8H6ClNO4 215.00.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384930B2
Source datasetuspto-grants-2008_06
ORD IDord-42ae182cd62e416c9cf1bbffc445fb92
Source noteuspto-grants-2008_06