HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621730Generated: October 27, 2026
Methanol → Methyl 3,5-dihydroxy-6,8-decadienoate
https://huagongshe.com/reaction/621730
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Triethylborane | HCID 7357 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 3-hydroxy-5-oxo-6,8-decadienoate | HCID 54125930 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 3,5-dihydroxy-6,8-decadienoate | HCID 53818818 | 42.7% |
Reaction Steps
To a cold (-15° C.) solution of methyl 3-hydroxy-5-oxo-6,8-decadienoate (18.5 g, 86.9 mmol) in THF (300 mL) was added triethylborane (1M in THF, 113 mL, 113 mmol) and the solution was stirred for 20 minutes. After the mixture was cooled to -78° C., NaBH4 (6 g, 159 mmol) and methanol (37.5 mL) were added. The solution was vigorously stirred for 30 minutes at -78° C. and at ambient temperature for 3 hours. The solvent was removed under reduced pressure and the residue was partitioned between 1N HCl and ethyl acetate. The organic layer was dried (Na2SO4) and concentrated. The residue was purified by chromatography on silica gel (diethyl ether:hexane/3:1) to afford 7.95 g (42.7%) of the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04824959 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-cbb898819306481984147b9938f914d7 |
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| Source note | uspto-grants-1989_04 |
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