HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865753Generated: October 31, 2026
Trimethylsilyldiazomethane → HCID 44248134, compound
https://huagongshe.com/reaction/1865753
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | HCID 86596612 | HCID 86596612 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 44248134 | HCID 44248134 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07626023B2 |
|---|
| Source dataset | uspto-grants-2009_12 |
|---|
| ORD ID | ord-e629c45f7f2d4d97a5ddbb59b23bbcc5 |
|---|
| Source note | uspto-grants-2009_12 |
|---|