HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427467Generated: November 1, 2026
Ammonium Hydroxide → 2-Azaspiro(4.5)decan-1-one
https://huagongshe.com/reaction/2427467
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-Cyanomethyl-cyclohexanecarboxylic acid methyl ester | HCID 57657808 | — |
| Catalyst | Dichlorocobalt hexahydrate | HCID 517166 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Azaspiro(4.5)decan-1-one | HCID 25067265 | 54% |
Reaction Steps
A 0° C. mixture of 1-cyanomethyl-cyclohexanecarboxylic acid methyl ester (4.28 g, 23.6 mmol) and cobalt (II) chloride hexahydrate (2.81 g, 11.8 mmol) in THF (80 mL) and water (40 mL) is treated portion-wise with sodium borohydride (4.47 g, 0.118 mol) and is warmed to room temperature and stirred for 48 hours under N2. The reaction is treated with 28% ammonium hydroxide (3.1 mL) and filtered through hyflo. The solvent is removed from the filtrate in vacuo and the residue is diluted with minimal water and brine and is extracted three times with 3:1 chloroform:isopropanol. The organic layer is dried (Na2SO4) and the solvent is removed in vacuo to afford crude product that is purified with a 0 to 10% methanol in CH2Cl2 gradient on silica gel to afford 1.95 g (54%) of the titled product. Rf=0.46 (9/1 CH2Cl2/methanol). MS (m/z): 154 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968585B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-bed85244ca7243c380e7309d2978f070 |
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| Source note | uspto-grants-2011_06 |
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