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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Spiro(4.5)decan-6-one | HCID 290662 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Ethynylspiro[4.5]decan-6-ol | HCID 86647580 | 79% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09012391B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-d1b6a3a1036942179ccdc93f7ed5bad7 |
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| Source note | uspto-grants-2015_04 |
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