HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622862Generated: October 30, 2026
Sodium Hydroxide → HCID 14152348, compound
https://huagongshe.com/reaction/622862
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | [3-(Hex-5-en-1-yl)oxiran-2-yl]methanol | HCID 14152344 | — |
| Reactant | Sodium bis(2-methoxyethoxy)aluminiumhydride | HCID 21584525 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14152348 | HCID 14152348 | 89% |
Reaction Steps
2 ml of a 3.4 molar solution sodium bis-(2-methoxyethoxy)-aluminum hydride (Red-AlR) (6.8 mM) are slowly added to a solution of 0.61 g (3.91 mM) 2S, 3S-2-epoxy-1-hydroxynon-8-ene (III) in 100 ml tetrahydrofuran at 0° C. in an argon gas atmosphere with agitation. After the addition, the mixture is allowed to react 3 hours at 0° C. and the reaction solution is subsequently left overnight at 25° C. After a careful addition of 5 ml 1 molar sodium hydroxide solution, the mixture is allowed to react one more hour with agitation. The organic phase is separated off and the aqueous phase is washed with 30 ml ether. The combined organic phases are washed with saturated sodium chloride solution, dried over magnesium sulfate and subsequently the solvent is evaporated in a vacuum. Bulb tube distillation at 130° C./0.5 mm pressure yields 0.54 g (3.42 mM) 1,3(S)-dihydroxynon-8-ene (IV) with a melting point of approximately 20° C. This corresponds to a yield of 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04772727 |
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| Source dataset | uspto-grants-1988_09 |
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| ORD ID | ord-91c8f19c715a4e8c9bebee7740ea9b48 |
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| Source note | uspto-grants-1988_09 |
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