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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290983Generated: October 28, 2026

Formaldehyde → t-Butyl 4-(succinimidomethylamino)phenoxyacetate

https://huagongshe.com/reaction/1290983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSuccinimideHCID 11439—
ReactantTert-butyl 2-(4-aminophenoxy)acetateHCID 22060435—
SolventEthanolHCID 702—
Productt-Butyl 4-(succinimidomethylamino)phenoxyacetateHCID 1061670584%

Reaction Steps

t-Butyl 4-aminophenoxyacetate (7.00 g, 31.4 mmol) and succinimide (3.11 g, 31.4 mmol) were added to ethanol (40 ml), and a 37% aqueous formaldehyde solution (2.55 g, 31.4 mmol) was added. The mixtue was refluxed under heating for 4 hours. Low boiling matters were distilled away from the reaction mixture under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate) to give 8.37 g of t-butyl 4-(succinimidomethylamino)phenoxyacetate as a yellow solid (84%). This solid (8.30 g, 26.0 mmol) was dissolved in dimethyl sulfoxide (50 ml) and sodium borohydride (989 mg, 26.0 mmol) was added, which was followed by stirring at 100° C. for 30 minutes. After cooling, water was poured into the reaction mixture and the mixture was extracted with diethyl ether. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. After filtration, low boiling matters were distilled away from the filtrate under reduced pressure and the residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=1/1) to give 3.62 g of t-butyl 4-(methylamino)phenoxyacetate as a yellow oil (59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753670
Source datasetuspto-grants-1998_05
ORD IDord-ab375f6607914d07926bd25231293dde
Source noteuspto-grants-1998_05