Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant9-(3,4-Dichlorophenyl)-3-azaspiro[5.5]undec-8-eneHCID 16006326—
ReactantDichloromethane methanolHCID 21226129—
SolventMethanolHCID 887—
Solvent1,1-DichloroethaneHCID 6365—
ProductAmmonium HydroxideHCID 149231%
Product9-(3,4-Dichloro-phenyl)-3-methyl-3-aza-spiro[5.5]undec-8-eneHCID 16006435105.1%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093388B2
Source datasetuspto-grants-2012_01
ORD IDord-1f3b281e26c54128b69c48a8d55c379b
Source noteuspto-grants-2012_01