HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903480Generated: October 30, 2026
Sodium Methoxide → HCID 23335969, compound
https://huagongshe.com/reaction/903480
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 23335967 | HCID 23335967 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23335969 | HCID 23335969 | — |
Reaction Steps
To a stirred solution of 5.47 g. (0.02 mole) of 3-chloro-N-isopropyl-4-methyl-2,6-dinitroaniline in 100 ml. of methanol is added 1.79 g. (0.033 mole) of sodium methoxide. The reaction mixture is stirred at reflux for three hours, cooled to room temperature and filtered. The filtrate is evaporated at reduced pressure and the residue partitioned between ether and dilute aqueous hydrochloric acid. The organic phase is successively washed with water, saturated sodium bicarbonate and brine. It is then dried over anhydrous magnesium sulfate. Evaporation of the solvent in vacuo gives 5.0 g. of the desired product having a m.p. of 72°-77° C. Two recrystallizations from methanol give the analytical sample, m.p. 77.5°-79° C. Analysis: Calcd. for C11H15N3O5 : C, 49.07; H, 5.62; N, 15.61. Found: C, 49.35; H, 5.66; N, 15.77.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04227913 |
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| Source dataset | uspto-grants-1980_10 |
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| ORD ID | ord-48a4f67d438b4c6aba24a30abfdb06c0 |
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| Source note | uspto-grants-1980_10 |
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