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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681061Generated: November 4, 2026

Bromotrimethylsilane → HCID 9942900, compound

https://huagongshe.com/reaction/1681061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromotrimethylsilaneHCID 76113—
ReactantHCID 86746394HCID 86746394—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 9942900HCID 9942900—

Reaction Steps

A solution of [(E)-4-[(2-amino-3,4-dioxo-1-cyclobuten-1-yl)amino]-2-butenyl]phosphonic acid diethyl ester (1.0 g, 3.3 mmol) and bromotrimethylsilane (4.6 mL, 35 mmol) in anhydrous 1,2-dichloroethane (30 mL) under nitrogen was refluxed for 20 minutes and then cooled and evaporated. The residue was dissolved in water (150 mL) and washed with diethyl ether (2×75 mL). The resulting material, upon concentrating the aqueous layer, was recrystallized from methanol in ethyl acetate (final volume=100 mL) to yield [(E)-4-[(2-amino-3,4-dioxo-1-cyclobuten-1-yl)amino]-2-butenyl]phosphonic acid one third hydrate as a yellow solid (0.59 g, 71%, mp 220°-230° C. (dec)); IR (KBr, cm-1): 3280, 3100, 1800, 1640; MS (-FAB): 245 (M-H); 1H NMR (DMSO, 400 MHz): δ 7.47 (br s, 3 NH), 5.63-5.58 (m, 2H), 4.10 (br s, 2H), 2.38 (d of d, J=21 and 6 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05168103
Source datasetuspto-grants-1992_12
ORD IDord-c883176f7d3448cc94a020dde1ddd230
Source noteuspto-grants-1992_12