HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045403Generated: October 25, 2026
Isopropanol → 2-(benzyloxymethyl)-3,4-dihydro-2H-pyran
https://huagongshe.com/reaction/1045403
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ((2-(Allyloxy)pent-4-enyloxy)methyl)benzene | HCID 12996273 | — |
| Catalyst | Grubbs Catalyst | HCID 6392641 | — |
| Catalyst | Benzylidenebis(tricyclohexylphosphine)dichlororuthenium | HCID 11967259 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(benzyloxymethyl)-3,4-dihydro-2H-pyran | HCID 4095658 | — |
Reaction Steps
Benzylidene-bis(tricyclohexylphosphine)dichlororuthenium, bis(tricyclohexylphosphine) benzylidine ruthenium(IV) chloride—Grubbs 1 generation catalyst (0.5 g, 0.54 mmol) was added in one portion to a stirred solution of ((2-(allyloxy)pent-4-enyloxy)methyl)benzene (12) (4 g, 17.2 mmol) in toluene (200 mL). The resulting mixture was heated at 50° C. under N2 for 2 hours before isopropanol (18 mL) and NaOH (0.17 g) were added. The mixture was then heated at 120° C. overnight. The solvent was evaporated and the residue was purified over silica gel using Et2O and hexane to give 2-(benzyloxymethyl)-3,4-dihydro-2H-pyran (13).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569283B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-4c0b433d4a6b4a059af057edae0e945c |
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| Source note | uspto-grants-2013_10 |
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