HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419281Generated: October 29, 2026
Formaldehyde → 9-(3,4-Dichloro-phenyl)-3-methyl-3-aza-spiro[5.5]undec-8-ene
https://huagongshe.com/reaction/419281
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 9-(3,4-Dichlorophenyl)-3-azaspiro[5.5]undec-8-ene | HCID 16006326 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | Ammonium Hydroxide | HCID 14923 | 1% |
| Product | 9-(3,4-Dichloro-phenyl)-3-methyl-3-aza-spiro[5.5]undec-8-ene | HCID 16006435 | 105.1% |
Reaction Steps
To an ice cooled solution of 9-(3,4-dichloro-phenyl)-3-aza-spiro[5.5]undec-8-ene (410 mg, 1.38 mmol) in dichloroethane (12 mL) and methanol (4 mL), formaldehyde (37% in water, 157 μL, 2.08 mmol) was added and stirred for 1 h at 0° C. Sodium triacetoxy-borohydride (585 mg, 2.76 mmol) was added and the mixture stirred at room temperature over night. The reaction was quenched with aqueous sodium hydrogen-carbonate and evaporated. The remaining aqueous phase was extracted four times with dichloromethane and the combined organic phase was dried (sodium sulfate), filtered and evaporated to give 320 mg of crude material. Flash chromatography (dichloromethane/methanol 9:1 with 1% ammonium hydroxide) gave 225 mg (52%) of 9-(3,4-dichloro-phenyl)-3-methyl-3-aza-spiro[5.5]undec-8-ene as an yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093388B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-1f3b281e26c54128b69c48a8d55c379b |
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| Source note | uspto-grants-2012_01 |
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