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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374277Generated: November 1, 2026

Benzylamine → N-Benzyl-1,4-dioxaspiro[4.5]decan-8-amine

https://huagongshe.com/reaction/1374277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantSodium HydroxideHCID 14798—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
ProductN-Benzyl-1,4-dioxaspiro[4.5]decan-8-amineHCID 11791515100%

Reaction Steps

1,4-cyclohexanedione ethylene ketal (5.00 g, 32.0 mmol, 1 eq.), sodium triacetoxyborohydride (8.14 g, 38.4 mmol, 1.2 eq.) and benzylamine (3.50 mL, 32.0 mmol, 1 eq.) were mixed in methylene chloride (100 mL) at room temperature. Stirred for 20 hours. Added 50 mL of 1.0 N NaOH. Stirred for 10 minutes. Extracted 3 times with methylene chloride (50 mL). The organic layers were combined, dried over sodium sulfate and stripped to give N-(phenylmethyl)-1,4-Dioxaspiro[4.5]decan-8-amine (7.91 g) of a light amber oil as product. Yield=100%. LCMS detects (M+H)+=248.26.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163937B2
Source datasetuspto-grants-2007_01
ORD IDord-11a780f1347f4ec688bb5fbdb544f51c
Source noteuspto-grants-2007_01