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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865753Generated: October 31, 2026

Trimethylsilyldiazomethane → HCID 44248134, compound

https://huagongshe.com/reaction/1865753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantHCID 86596612HCID 86596612—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 44248134HCID 4424813488%

Reaction Steps

To a 0° C. (ice water bath) solution of 3-phenyl-3-methyl-2-oxobutanoate (9.0 g, 47 mmol, from Reference Example 35) in ether (40 mL) and methanol (60 mL). Trimethylsilyl diazomethane (2.0 M solution in hexanes, 35 mL, 70 mmol, Aldrich) is added dropwise until the evolution of gas ceased and the yellow color of the reagent persisted in solution. The solvents are evaporated under reduced pressure and the residue is taken up in ether/hexanes (1:1) and washed with 2% aqueous hydrochloric acid, saturated aqueous sodium bicarbonate solution, and saturated aqueous sodium chloride solution. The combined extracts are then dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give a straw-colored liquid (8.5 g, 88%). MS (ES+): (M+H)=206.9

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07626023B2
Source datasetuspto-grants-2009_12
ORD IDord-e629c45f7f2d4d97a5ddbb59b23bbcc5
Source noteuspto-grants-2009_12