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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229149Generated: October 30, 2026

Trimethylsilyldiazomethane → HCID 18466584, compound

https://huagongshe.com/reaction/2229149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantHCID 18466562HCID 18466562—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
ProductHCID 18466584HCID 18466584102.2%

Reaction Steps

To 2-(4-{4-[(t-butyl)oxycarbonyl]piperazinyl}-3-fluorophenyl)acetic acid (0.3 g, 1.0 mmol) in 2 mL methanol and 7 mL benzene was added trimethylsilyidiazomethane (0.65 mL, 1.30 mmol). After stirring at ambient temperature for 1 hour, the reaction mixture was concentrated to provide 0.36 g (99%) of the title compound. 1H NMR (CDCl3; 300 MHz) δ7.00 (m, 2H), 6.90 (t, J=8.3 Hz, 1H), 3.71 (s, 3H), 3.61 (t, J=4.9 Hz, 4H), 3.57 (s, 2H), 3.02 (t, J=5.0 Hz, 4H), 1.50 (s, 9H); ESI (M+H)+=353.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420349B1
Source datasetuspto-grants-2002_07
ORD IDord-599cb0507be545199b519c7325d0e47c
Source noteuspto-grants-2002_07