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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58341Generated: October 25, 2026

Ammonia → (4-{[4-(Methylamino)butanoyl]amino}butyl)(triphenyl)phosphonium bromide

https://huagongshe.com/reaction/58341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
Reactant11,14,14-Trimethyl-7,12-dioxo-1,1,1-triphenyl-13-oxa-6,11-diaza-1-phosphoniapentadecane bromideHCID 117773664—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(4-{[4-(Methylamino)butanoyl]amino}butyl)(triphenyl)phosphonium bromideHCID 8946281589.6%

Reaction Steps

11,14,14-trimethyl-7,12-dioxo-1,1,1-triphenyl-13-oxa-6,11-diaza-1-phosphoniapentadecane bromide (910 mg, 1.50 mmol) was dissolved in methylene chloride (4.6 mL) and methanol (0.50 mL). The solution at room temperature was treated with 2.0 M hydrogen chloride in diethyl ether (1.63 mL, 3.26 mmol). The mixture was stirred overnight at room temperature, then cooled with an ice bath and treated with 7N ammonia in methanol (0.61 mL, 4.30 mmol). After 30 minutes, the slurry that resulted was filtered, and the solids were washed with methylene chloride. The filtrate was concentrated to give the title compound (690 mg, 91%, 91% pure) as a white foam. The product of step 2 was used crude in next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434753B2
Source datasetuspto-grants-2016_09
ORD IDord-0cfcf14d2fc74acc94f03bcc30aa4eb3
Source noteuspto-grants-2016_09