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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3-Chloro-2-nitrobenzoic acid | HCID 20902 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Solvent | Acetonitrile methanol | HCID 21959252 | — |
| Product | Methyl 3-chloro-2-nitrobenzoate | HCID 12187125 | 74.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07384930B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-42ae182cd62e416c9cf1bbffc445fb92 |
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| Source note | uspto-grants-2008_06 |
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