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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622862Generated: October 30, 2026

Sodium Hydroxide → HCID 14152348, compound

https://huagongshe.com/reaction/622862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant[3-(Hex-5-en-1-yl)oxiran-2-yl]methanolHCID 14152344—
ReactantSodium bis(2-methoxyethoxy)aluminiumhydrideHCID 21584525—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14152348HCID 1415234889%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04772727
Source datasetuspto-grants-1988_09
ORD IDord-91c8f19c715a4e8c9bebee7740ea9b48
Source noteuspto-grants-1988_09