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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277193Generated: October 31, 2026

Putrescine → HCID 57517491, compound

https://huagongshe.com/reaction/2277193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPutrescineHCID 1045—
ReactantAmmonium ChlorideHCID 25517—
ReactantN-FluorobenzenesulfonimideHCID 588007—
ReactantCarbamic acid, (2,4-dimethoxyphenyl)-, 1,1-dimethylethyl esterHCID 10610880—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57517491HCID 5751749138.2%

Reaction Steps

To a solution of tert-butyl (2,4-dimethoxyphenyl)carbamate (7.09 g) and tetramethylenediamine (12.7 mL) in THF (70 mL) was added 1.6 M n-butyllithium hexane solution (52.5 mL) at −78° C., and the mixture was stirred at the same temperature for 20 min, and then at room temperature for 45 min. To the reaction mixture was added a solution of N-fluoro-N-(phenylsulfonyl)benzenesulfonamide (12.8 g) in THF (30 mL) at −78° C., and the mixture was allowed to warm to room temperature, and stirred overnight. To the reaction mixture was added saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (2.90 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133129B2
Source datasetuspto-grants-2015_09
ORD IDord-76ceb327c32b4399a9bd0b400086f7d9
Source noteuspto-grants-2015_09