HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616303Generated: October 25, 2026
2,4-Dinitrophenol → 1-Methoxy-3-methyl-1-[(3-methylbut-2-en-1-yl)oxy]but-2-ene
https://huagongshe.com/reaction/616303
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4-Dinitrophenol | HCID 1493 | — |
| Reactant | 3-Methyl-2-buten-1-OL | HCID 11173 | — |
| Reactant | 1,1-Dimethoxy-3-methyl-2-butene | HCID 11040731 | — |
| Product | 1-Methoxy-3-methyl-1-[(3-methylbut-2-en-1-yl)oxy]but-2-ene | HCID 22748295 | — |
Reaction Steps
In a 50 ml. one-neck flask was placed 5.5 g. (0.0422 mol.) of 1,1-dimethoxy-3-methyl-2-butene and 10.0 g. (0.116 mol.) of prenol and 0.40 g. (0.002 mol.) of 2,4-dinitrophenol. The resulting solution was degassed with nitrogen and sealed with a serum cap and stirred at room temperature for 76 hours. The reaction solution was then diluted with 100 ml. of hexane and washed with 3 × 100 ml. of 1.0 N aqueous NaOH solution and 2 × 100 ml. of saturated aqueous NaCl solution. The combined water washings were back with extracted 1 × 50 ml. of hexane. The combined hexane solutions were dried (Na2SO4) and concentrated to give 9.0 g. of crude product. Distillation of 8.3 g. at 20 mmHg and a bath temperature of 55°-60° gave 1.48 g. of prenol. Continued distillation initially at 0.20 mmHg gave 2.43 g. of 1-methoxy-1-(3-methylbut-2-enoxy)-3-methyl-2-butene (b.p. 40°-45° at 0.02 mmHg) and finally at 0.050 mmHg gave 3.29 g. of 1,1-bis-(3-methylbut-2-enoxy)-3-metylbut-2-ene (b.p. 70°-75° at 0.050 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04073811 |
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| Source dataset | uspto-grants-1978_02 |
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| ORD ID | ord-1ee98b19cef14a469be32f1fdbfad19b |
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| Source note | uspto-grants-1978_02 |
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