HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414831Generated: November 1, 2026
Methyl iodide → 6-[(6-Methoxy-3,7,7-trimethyloct-2-en-1-yl)oxy]-2,3-dihydro-1-benzofuran
https://huagongshe.com/reaction/1414831
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-[(6-Hydroxy-3,7,7-trimethyl-2-octenyl)-oxy]-2,3-dihydrobenzofuran | HCID 53891706 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | 6-[(6-Methoxy-3,7,7-trimethyloct-2-en-1-yl)oxy]-2,3-dihydro-1-benzofuran | HCID 53713182 | — |
Reaction Steps
0.4 g. of 6-[(6-hydroxy-3,7,7-trimethyl-2-octenyl)-oxy]-2,3-dihydrobenzofuran are dissolved in 10 ml. of absolute tetrahydrofuran and, while stirring, warmed to 40° C. for 2 hours with 0.5 g. of a 55% by weight sodium hydride suspension in oil. Then 2 ml. of hexamethylphosphoric acid triamide and 1 ml. of methyl iodide are added and the mixture is stirred for 12 hours at room temperature. For the working up, the mixture is poured onto ice-water and extracted twice with diethyl ether. The ether extracts are washed with water and saturated aqueous sodium chloride solution, dried over sodium sulfate and evaporated. By chromatography on silica gel with hexane/diethyl ether (19:1 parts by volume) there is obtained 6-[(6-methoxy-3,7,7-trimethyl-2-octenyl)-oxy]-2,3-dihydrobenzofuran; nD25 = 1.5170.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04002647 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-274842afeed347d5824f8787e5d4a7f4 |
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| Source note | uspto-grants-1977_01 |
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