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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021414Generated: November 2, 2026

Dimethylamine → Tert-butyl 4-((dimethylamino)methyl)phenethylcarbamate

https://huagongshe.com/reaction/1021414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86653235HCID 86653235—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-((dimethylamino)methyl)phenethylcarbamateHCID 6708040254%

Reaction Steps

To a stirred suspension of 4-(2-(tert-butoxycarbonylamino)ethyl)benzyl methanesulfonate (0.33 g, 1.0 mmol) and N,N-diisopropylethylamine (0.19 mL, 1.1 mmol) in tetrahydrofuran (50 mL) was added a 2M solution of dimethylamine in tetrahydrofuran (5.0 mL, 10 mmol). The resulting mixture was stirred in an oil bath set to 60° C. for 6 hours. The solution was cooled to ambient temperature and concentrated. The residue was partitioned between ethyl acetate (20 mL) and water (10 mL). The organic layer was dried over sodium sulfate and concentrated. The residue was purified by chromatography on silica gel, eluting with 99/1 to 98/2 chloroform/(90/10 methanol/concentrated ammonium hydroxide), to afford tert-butyl 4-((dimethylamino)methyl)phenethylcarbamate as a colorless oil (0.15 g, 54% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716498B2
Source datasetuspto-grants-2014_05
ORD IDord-15babc6428934a1889457fa2af0b9810
Source noteuspto-grants-2014_05