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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548941Generated: October 27, 2026

1,1-Dichloroethane → Tert-butyl 9-methyl-3,9-diazaspiro[5.5]undecane-3-carboxylate

https://huagongshe.com/reaction/548941

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DichloroethaneHCID 6365—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl 3,9-diazaspiro[5.5]undecane-3-carboxylateHCID 15296367—
SolventWaterHCID 962—
ProductAmmonium HydroxideHCID 149231%
ProductTert-butyl 9-methyl-3,9-diazaspiro[5.5]undecane-3-carboxylateHCID 5880817954%

Reaction Conditions

Temperature0 °C

Reaction Steps

To an ice cooled solution of 3,9-diaza-spiro[5.5]undecane-3-carboxylic acid tert-butyl ester (1.55 g, 6 mmol) in dichloroethane (50 mL) formaldehyde (0.68 mL, 9 mmol) was added and stirred for 1 h at 0° C. Sodium triacetoxyborohydride (2.54 g, 12 mmol) was added and the reaction stirred at room temperature over night. Aqueous sodium hydrogencarbonate (sat. 50 mL) and water (50 mL) were added and the aqueous phase extracted five times with dichloromethane. The combined organic phase was washed with brine, dried (sodium sulfate), filtered and evaporated. Flash chromatography (dichloromethane/methanol 9:1 with 1% ammonium hydroxide) gave 435 mg (27%) 9-methyl-3,9-diaza-spiro[5.5]undecane-3-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943630B2
Source datasetuspto-grants-2011_05
ORD IDord-902bcdbedc3347739f3f0bce9abaae64
Source noteuspto-grants-2011_05