HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070572Generated: November 4, 2026
HCID 57771564, compound → HCID 57771601, compound
https://huagongshe.com/reaction/2070572
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57771564 | HCID 57771564 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57771601 | HCID 57771601 | 59.3% |
Reaction Steps
To a solution of spiro[4.5]dec-1-en-2-yl-methanol (50 mg) obtained in Step 5 of Example 15 in tetrahydrofuran (1 mL) was added 5% palladium carbon (5 mg), followed by stirring the reaction mixture under normal pressure in an atmosphere of hydrogen at room temperature for 20 hours. Then, the reaction mixture was filtered through Celite and the filtrate was concentrated. The residue was dissolved in methanol (1 mL). To the solution was added sodium borohydride (10 mg), followed by stirring the reaction mixture at room temperature for 1 hour. Then, after addition of 1N aqueous hydrochloric acid solution, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water, dried and concentrated to give spiro[4.5]dec-2-yl-methanol (30 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299296B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-6808e96ef8924701b9586fac715501fd |
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| Source note | uspto-grants-2012_10 |
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