HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802515Generated: October 27, 2026
4-Methylbenzaldehyde → 8-(3-Hydroxy-3-(p-tolyl)propyn-1-yl)-1,4-dioxaspiro[4.5]decan-8-ol
https://huagongshe.com/reaction/1802515
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylbenzaldehyde | HCID 7725 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 8-Ethynyl-1,4-dioxaspiro[4.5]decan-8-ol | HCID 11105985 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-(3-Hydroxy-3-(p-tolyl)propyn-1-yl)-1,4-dioxaspiro[4.5]decan-8-ol | HCID 58399358 | 71.1% |
Reaction Steps
To a solution of 8-ethynyl-1,4-dioxaspiro[4.5]decan-8-ol (Reference Example 1) (15.0 g, 82.3 mmol) in tetrahydrofuran (165 mL), 2.77 M n-butyllithium (solution in n-hexane, 62.4 mL, 172.9 mmol) was added dropwise at −72° C. for 25 minutes, and the obtained solution was stirred at the same temperature for 30 minutes. Thereafter, p-tolualdehyde (10.2 mL, 86.4 mmol) was added dropwise at −72° C. for 5 minutes, and the obtained solution was stirred at the same temperature for 30 minutes. The reaction solution was allowed to warm to room temperature and poured into saturated aqueous ammonium chloride solution. The reaction solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel, n-hexane/ethyl acetate) to obtain the captioned compound (17.7 g, 58.5 mmol, 71%) as an amorphous product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08349874B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-c78dccd1bae4486e8092a72005327a66 |
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| Source note | uspto-grants-2013_01 |
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