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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970976Generated: November 2, 2026

Benzylamine → N-(7-methyl-1,4-dioxaspiro[4.5]dec-8-ylidene)-1-phenylmethanamine

https://huagongshe.com/reaction/1970976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl methyl etherHCID 15413—
Reactant7-Methyl-1,4-dioxaspiro[4.5]decan-8-oneHCID 270628—
CatalystTitanium TetrachlorideHCID 24193—
SolventDichloromethaneHCID 6344—
ProductN-(7-methyl-1,4-dioxaspiro[4.5]dec-8-ylidene)-1-phenylmethanamineHCID 67536022—

Reaction Steps

To a solution of NEt3 (560 mL, 4.02 mol) and benzylamine (131 mL, 1.20 mol) in CH2Cl2 (500 mL) was added TiCl4 (500 mL of 1.0 M solution in CH2Cl2, 0.500 mol) over 30 min while the internal temperature was kept below −10° C. The resulting dark red suspension was stirred at −20° C. to −30° C. for 15 min, then a solution of 7-methyl-1,4-dioxaspiro[4.5]decan-8-one (170 g, 1.00 mmol) in CH2Cl2 (500 mL) was added at −10° C. The resulting grey-yellow suspension was allowed to warm to room temperature over 2 h, then stirred at room temperature for 16 h. MTBE (1.0 L) was added to the reaction mixture, and the yellow suspension was stirred at room temperature for 30 min and filtered through a pad of Solka Floc. The cake was washed with MTBE (4×500 mL), and the combined filtrates were concentrated to provide N-(7-methyl-1,4-dioxaspiro[4.5]dec-8-ylidene)-1-phenylmethanamine, which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431569B2
Source datasetuspto-grants-2013_04
ORD IDord-9c4e65b9df92429fa27ef8e2dcb0b653
Source noteuspto-grants-2013_04