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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471370Generated: October 31, 2026

Hydrochloric Acid → 6-Ethynylspiro[4.5]decan-6-ol

https://huagongshe.com/reaction/1471370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCyclohexanoneHCID 7967—
Reactant1,4-DibromobutaneHCID 8056—
ReactantAmmonium ChlorideHCID 25517—
ReactantSpiro(4.5)decan-6-oneHCID 290662—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product6-Ethynylspiro[4.5]decan-6-olHCID 8664758079%

Reaction Conditions

Temperature20 °C

Reaction Steps

At 5° C., a solution of lithium acetylide ethylene diamine complex (200 g, 2.17 mol) in THF (1 l) was treated dropwise with a solution of spiro[4.5]decan-6-one (196 g, 1.29 mol, prepared from cyclohexanone and 1,4-dibromobutane in the presence of potassium tert.-butylate in toluene) in THF (0.8 l). The resulting mixture was stirred for 3 h at 20° C., poured into a saturated aqueous solution of NH4Cl, acidified with conc. HCl and extracted three time with MTBE (500 ml). The aqueous phase was extracted twice with MTBE (150 ml) and the combined organic phases were washed twice with water (500 ml), once with a saturated aqueous solution of NaCl, dried (MgSO4), and concentrated. Short-path Vigreux-distillation (0.08 mbar, bath temperature: 140° C., head temp.: 100-105° C.) of the crude product (257 g) gave 6-ethynylspiro[4.5]decan-6-ol (180.8 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012391B2
Source datasetuspto-grants-2015_04
ORD IDord-d1b6a3a1036942179ccdc93f7ed5bad7
Source noteuspto-grants-2015_04