HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246807Generated: November 2, 2026
2-Methyl-4-nitroaniline → HCID 11535999, compound
https://huagongshe.com/reaction/2246807
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-4-nitroaniline | HCID 7441 | — |
| Reactant | 2,2-Dichloro-1,4-dioxane | HCID 12424325 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11535999 | HCID 11535999 | — |
Reaction Steps
1.05 g of a mixture of 2-chlorodioxene and 2,2-dichlorodioxane (molar ratio 1:1) are added to a solution of 1.10 g (7.24 mmol) of 2-methyl-4-nitroaniline in 20 ml of THF, and the mixture is heated to the boil. The solvent is distilled off, and the residue, a brown viscous liquid, is heated at 80° C. for 18 hours. After cooling, the residue is recrystallised from toluene/tert-butyl methyl ether: 1.50 g of 2-(2-chloroethoxy)-N-(2-methyl-4-nitrophenyl)acetamide as yellowish crystals, m.p. 113-114° C. 1H-NMR (d6-DMSO): δ=2.35 (s; 3H), 3.82 (m; 4H), 4.23 (s; 2H), 8.05 (d, J=8 Hz, 1H) 8.09 (dd, J=9 Hz, J=1 Hz, 1H), 8.16 (d, J=1 Hz, 1H), 9.33 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687624B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-03d20fd6836a4134b32f5bf29f7c0cac |
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| Source note | uspto-grants-2010_03 |
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