HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732563Generated: October 25, 2026
3-Methyl-3-buten-1-ol → 3-Methyl-2-buten-1-OL
https://huagongshe.com/reaction/1732563
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Methyl-3-buten-1-ol | HCID 12988 | — |
| Reactant | 2-Hydroxy-4-methyltetrahydropyran | HCID 11469063 | — |
| Product | 3-Methyl-2-buten-1-OL | HCID 11173 | — |
| Product | 3-Methylbutanal | HCID 11552 | — |
Reaction Steps
The autoclave was charged with 350 ml of a dioctyl phthalate solution containing 4.0 mg (0.00054 mml) of Rh4 (CO)12 and 0.173 g (0.856 mml) of ##STR23## and with 130 g (1.512 moles) of 2-methyl-1-buten-4ol. After thoroughly purging the autoclave with a mixed H2 /CO gas (1/1 in molar ratio), the reaction was carried out at a pressure of 140 kg/cm2 (absolute pressure) resulting from a mixed H2 /CO gas (1/1 in molar ratio) and at a temperature of 100° C., with stirring, for 4 hours. After the reaction, a very small amount of the reaction mixture was taken out and analyzed by gas chromatography, to show that 0.045 mole of the 2-methyl-1-buten-4-ol remained unreacted (the conversion being 97%), that the yield of 2-hydroxy-4-methyltetrahydropyran was 1.320 moles, and that the yields of 2-methyl-2-buten-4-ol and isovaleraldehyde were 0.058 and 0.073 mole, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04238419 |
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| Source dataset | uspto-grants-1980_12 |
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| ORD ID | ord-eaa6caf0b8f84013a43d54f391fb69ee |
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| Source note | uspto-grants-1980_12 |
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