HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918014Generated: October 30, 2026
Piperonyl alcohol → HCID 53700017, compound
https://huagongshe.com/reaction/918014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperonyl alcohol | HCID 10322 | — |
| Reactant | 18860-95-2 | HCID 205858 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 53700017 | HCID 53700017 | — |
Reaction Steps
8.7 g (0.05 mol) of sodium salt of the 3,4-methylendioxybenzylalcohol are added at 0° during the course of 15 minutes and while stirring to 12.5 g (0.055 mol) of 1,4-dibromo-2-methyl-2-butene which is dissolved in 100 cc of 1,2-dimethoxyethane. The mixture is stirred at 20°-25° for 16 hours and at 50° for 15 minutes. The solvent is then distilled off at reduced pressure and 100 cc amounts of water and ether are added to the residue. The aqueous phase is separated in a separatory funnel, the ether phase is extracted with saturated salt solution, is dried with sodium sulphate and evaporated. The residue is chromatographed on silica gel with hexane/ethyl acetate 9:1, whereby the 5-[(4-bromo-3-methyl-2-butenyloxy)-methyl]-1,3-benzodioxol is obtained as uniform colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03968235 |
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| Source dataset | uspto-grants-1976_07 |
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| ORD ID | ord-2153e432d0354693a29e547557d73ac0 |
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| Source note | uspto-grants-1976_07 |
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