HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424614Generated: October 30, 2026
Ethyl 1,4-dioxaspiro(4.5)decane-8-carboxylate → 1,4-Dioxaspiro(4.5)decane-8-carbaldehyde
https://huagongshe.com/reaction/424614
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 1,4-dioxaspiro(4.5)decane-8-carboxylate | HCID 10488810 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,4-Dioxaspiro(4.5)decane-8-carbaldehyde | HCID 9898947 | — |
Reaction Steps
Diisobutylaluminium hydride (1.5 M solution in toluene, 102 ml, 153 mmol) was added dropwise to a solution of 1,4-dioxa-spiro[4.5]decane-8-carboxylic acid ethyl ester (32.13 g, 150 mmol) in absol. toluene (160 ml) at −70 to −65° C. under argon and the mixture was stirred for 30 min. The mixture was then quenched at −70 to −60° C. by addition of methanol (80 ml). The reaction solution was warmed to RT, saturated sodium chloride solution (100 ml) was added and the reaction solution was filtered out with suction over kieselguhr. The kieselguhr was washed twice with ethyl acetate and the aqueous solution was separated off and extracted twice with ethyl acetate. The combined organic extracts were washed with saturated sodium chloride solution, dried over sodium sulfate and concentrated i. vac. Yield: 24.01 g (94%), yellow oil
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106055B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-e0aa159ddb29440db4e1f829d6de8ebd |
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| Source note | uspto-grants-2012_01 |
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