HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631542Generated: October 25, 2026
Trimethylsilyldiazomethane → HCID 53710760, compound
https://huagongshe.com/reaction/631542
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 4,4,4-Trifluoro-3-oxobutanenitrile | HCID 13843540 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 53710760 | HCID 53710760 | — |
Reaction Steps
(Trimethylsilyl)diazomethane (21 mL, 2M in diethyl ether) was added dropwise to a solution of 4,4,4-trifluoro-3-oxobutanenitrile (3.79 g, 26 mmol) in anhydrous diethyl ether (25 mL) previously cooled to 0° C. The resulting mixture was allowed to slowly warm to room temperatureand stirred overnight. The solvent was removed under reduced pressure to give 4,4,4-trifluoro-3-methoxybut-2-enenitrile, which was directly used in the next step without further purification. 1H NMR (300 MHz, CDCl3) δ 5.00 (s, 1H), 4.16 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09320739B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-31ffe4a07ccd42608be484e6a320e837 |
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| Source note | uspto-grants-2016_04 |
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