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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070584Generated: November 4, 2026

Hydrochloric Acid → Spiro[5.5]undec-1-ene-2-methanol

https://huagongshe.com/reaction/2070584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
ReactantSpiro[5.5]undec-1-ene-2-carboxylic acid methyl esterHCID 15701410—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
ProductSpiro[5.5]undec-1-ene-2-methanolHCID 5777155994%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of spiro[5.5]undec-1-ene-2-carboxylic acid methyl ester (2.07 g) obtained in Step 4 in tetrahydrofuran (30 mL) was added dropwise a 1M toluene solution of diisobutylaluminum hydride (30 mL) at −70° C. under argon atmosphere over 15 minutes, followed by stirring the reaction mixture at −70° C. for 1 hour. Then after careful addition of methanol (2 mL) and 6N aqueous hydrochloric acid solution (5 mL) to the reaction mixture, the temperature was raised to room temperature. The reaction mixture was poured into saturated brine, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine, dried and concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate:hexane (volume ratio)=1:5) to give spiro[5.5]undec-1-ene-2-methanol (1.685 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299296B2
Source datasetuspto-grants-2012_10
ORD IDord-c3bc6a26bcee471484d66f21d0a289ac
Source noteuspto-grants-2012_10