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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681063Generated: November 2, 2026

Bromotrimethylsilane → HCID 21972597, compound

https://huagongshe.com/reaction/1681063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromotrimethylsilaneHCID 76113—
ReactantHCID 57010612HCID 57010612—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 21972597HCID 2197259758%

Reaction Steps

A suspension of [2-[(2-amino-3,4-dioxo-1-cyclobuten-1-yl)methylamino]ethyl]phosphonic acid diethyl ester (660 mg, 2.3 mmol) in anhydrous 1,2-dichloroethane (20 mL) under nitrogen was treated with bromotrimethylsilane (2.0 mL, 15 mmol) and heated to reflux for 10 minutes. The yellow solution was concentrated and the resulting solid was dissolved in water (75 mL), washed with diethyl ether (2×50 mL) and evaporated. The solid was dissolved in boiling methanol, filtered, and concentrated with the addition of ethyl acetate to a final volume of 75 mL to afford the title compound as a yellow solid (310 mg, 58%, mp 230°-260° C. dec); IR (KBr, cm-1): 3340, 1800; MS (-FAB): 233 (M-H, 32), 148 (100); 1H NMR (DMSO, 400 MHz): δ 7.62 (br s, NH2), 3.68 (br s, 2H), 3.16 (br s, 3 H), 1.90 (d of t, J=18 and 7.5 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05168103
Source datasetuspto-grants-1992_12
ORD IDord-386ade9f70ff4714b75a5af5f42ac456
Source noteuspto-grants-1992_12