HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374394Generated: October 30, 2026
Water → 3-Dihydropyranyloxy-3-methyl butanol
https://huagongshe.com/reaction/374394
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Methyl beta-dihydropyranyloxyisovalerate | HCID 86749184 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Dihydropyranyloxy-3-methyl butanol | HCID 67733041 | 76.7% |
Reaction Steps
Thereafter, 0.7 g of lithium aluminum hydride was suspended in 20 ml of diethyl ether, and a solution of 1.98 g of methyl β-dihydropyranyloxyisovalerate in 3 ml of diethyl ether was slowly dropwise added to the suspension, and a reaction was allowed to proceed at room temperature overnight. The mixture was further heated and refluxed for 1 hr and then cooled, and 0.7 ml of water, 0.7 ml of a 15% aqueous sodium hydroxide solution and 2.1 ml of water were successively added in that order with ice cooling. The mixture was stirred at room temperature for 1 hr, 20 ml of tetrahydrofuran was added thereto, and the mixture was stirred for additional one hr. The precipitat was collected by filtration and washed with 10 ml of tetrahydrofuran, and the washing was combined with the filtrate. The solvent was removed from the combined filtrate and washing by distillation under a reduced pressure to obtain 1.32 g of crude 3-dihydropyranyloxy-3-methyl butanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05480580 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-657b72b2d2454ca09ddeda17bccb981e |
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| Source note | uspto-grants-1996_01 |
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