HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582052Generated: October 31, 2026
Methanol → Methyl 2-(3-nitrophenyl)acetate
https://huagongshe.com/reaction/582052
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | 3-Nitrophenylacetic acid | HCID 15876 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Product | Methyl 2-(3-nitrophenyl)acetate | HCID 526967 | — |
Reaction Steps
Combine (3-nitrophenyl)acetic acid (20.0 g, 110 mmol) and anhydrous methanol (125 mL). Add 7 drops of concentrated sulfuric acid. Heat to 50° C. After 14 hours, cool to ambient temperature. Evaporate in vacuo to give a residue. Partition the residue between water and diethyl ether. Separate the organic layer and extract with aqueous saturated sodium bicarbonate solution and brine. Dry the organic layer over MgSO4 and filter. Slowly evaporate to give methyl (3-nitrophenyl)acetate. 1H NMR (CDCl3) δ 8.17 (d, 1 H, J=1.1 Hz), 8.14 (dd, 1 H, J=1.0, 7.7 Hz), 7.63 (dd, 1 H, J=1.1, 7.7 Hz), 7.52 (t, 1 H, J=7.7 Hz), 3.75 (s, 2 H), 3.73 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05922752 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-fd1cc45a9de241f59bbefe37dbeec852 |
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| Source note | uspto-grants-1999_07 |
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