HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465873Generated: October 29, 2026
Tetrahydrofuran → 5-methyl-1,5-hexanediol
https://huagongshe.com/reaction/465873
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Delta-Valerolactone | HCID 10953 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Product | 5-methyl-1,5-hexanediol | HCID 11137210 | 84% |
Reaction Steps
To 67 mL of a 3.0M solution of methylmagnesium bromide (201 mmol in ether) stirring at 0° C. under argon, was added dropwise a solution of valerolactone (5.0 g, 50 mmol) in 25 mL dry THF. A white precipitate was formed. After 30 minutes the reaction mixture was warmed up to room temperature. After 4.5 hours, the reaction was quenched with 12 mL of water and concentrated on a rotoevaporator. The residue was stirred with 50 mL EtOAc and 20 mL saturated aqueous NH4Cl. The 2 layers were separated. The aqueous layer was extracted twice more with EtOAc (50 mL each). The organic layers were combined and washed with brine, dried over MgSO4, and concentrated on a rotoevaporator to obtain 5.57 g (84%) of the title product. Rf is 0.35 in EtOAc; UV, Ce(SO4)2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05153327 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-490f425349b240f8b8e1c724d3c1d6bc |
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| Source note | uspto-grants-1992_10 |
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