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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048042Generated: October 31, 2026

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

https://huagongshe.com/reaction/1048042

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 numberUS08569522B2
Source datasetuspto-grants-2013_10
ORD IDord-3b9f1bfd1d35479c87125f59b386e59c
Source noteuspto-grants-2013_10