HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236223Generated: October 26, 2026
Methyl nitrate → 4-Bromo-2,6-dimethyl-N-nitroaniline
https://huagongshe.com/reaction/236223
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl nitrate | HCID 11724 | — |
| Reactant | 4-Bromo-2,6-xylidine | HCID 90549 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Bromo-2,6-dimethyl-N-nitroaniline | HCID 13106752 | 27.6% |
Reaction Steps
To a cooled (-60° C.) solution of 4-bromo-2,6-di-methylaniline (0.037 mole, 7.4 g) dissolved in anhydrous ether (100 ml) under nitrogen with stirring is added dropwise, phenyl lithium (21.5 ml, 0.040 mole). The solution is stirred for 1.5 hours at -60° C. The solution is allowed to warm to -10° C., then it is cooled to -60° C. The nitrogen flow is stopped while methyl nitrate (0.044 mole, 3.5 g) in anhydrous ether (25 ml) is added dropwise. The solution is stirred for 0.5 hour at -60° C., then it is allowed to warm to room temperature. The solution is stirred for 1.6 hours; the ether layer is evaporated. The solid is dissolved in water (250 ml), then is extracted with ether (2×100 ml). The cold water layer is acidified with 5% HCl. The precipitated product is filtered, washed with water, and dried in vacuo. Recrystallization from hot hexane yields 2.5 g of the desired product melting at 129°-131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04643755 |
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| Source dataset | uspto-grants-1987_02 |
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| ORD ID | ord-7c0325f366d14c15b34af987dd71e9f4 |
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| Source note | uspto-grants-1987_02 |
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