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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114254Generated: October 29, 2026

Bromotrimethylsilane → {2-[2-Ethyl-4-(6-ethyl-4-hydroxy-7-methyl-3-oxo-1,3-dihydro-isobenzofuran-5-yl)-but-2-enylamino]-ethyl}-phosphonic acid

https://huagongshe.com/reaction/2114254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromotrimethylsilaneHCID 76113—
Reactant(2-{2-Ethyl-4-[6-ethyl-7-methyl-3-oxo-4-(2-trimethylsilanyl-ethoxy)-1,3-dihydro-isobenzofuran-5-yl]-but-2-enyl amino}-ethyl)-phosphonic acid diethyl esterHCID 72563629—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product{2-[2-Ethyl-4-(6-ethyl-4-hydroxy-7-methyl-3-oxo-1,3-dihydro-isobenzofuran-5-yl)-but-2-enylamino]-ethyl}-phosphonic acidHCID 6701023444.7%

Reaction Steps

(2-{2-Ethyl-4-[6-ethyl-7-methyl-3-oxo-4-(2-trimethylsilanyl-ethoxy)-1,3-dihydro-isobenzofuran-5-yl]-but-2-enylamino}-ethyl)-phosphonic acid diethyl ester (24.9 mg, 0.045 mmol) was dissolved in DMF (0.5 mL) and DCM (0.5 mL). Trimethylsilyl bromide (68.7 mg, 0.449 mmol) was added and the reaction was stirred at room temperature. After 20 hours, the reaction was quenched with MeOH (0.15 mL). The solvents were evaporated in vacuo and the crude material was purified by RP-HPLC (eluent: water/MeCN). The product-containing fractions were combined and lyophilized to yield 8.0 mg of the free phosphonic acid [MS: 498 M++1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432261B2
Source datasetuspto-grants-2008_10
ORD IDord-bd2f371d93404abc95eb1dd076287020
Source noteuspto-grants-2008_10