HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292348Generated: November 1, 2026
N-methyl-N-(trimethylsilyl)trifluoroacetamide → HCID 56974509, compound
https://huagongshe.com/reaction/2292348
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-methyl-N-(trimethylsilyl)trifluoroacetamide | HCID 32510 | — |
| Reactant | 3,4-Dihydroxybenzohydrazide | HCID 586300 | — |
| Reactant | Phenylmethyl 2-(chlorocarbonyl)hydrazinecarboxylate | HCID 21681927 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 56974509 | HCID 56974509 | — |
Reaction Steps
19.52 ml (0.10 mol) of N-methyl-N-trimethylsilyltrifluoroacetamide was added to a suspension of 4.20 g (0.025 mol) of 3,4-dihydroxybenzoic acid, hydrazide in 25 ml of dry acetonitrile. Stirring was continued at room temperature until a clear solution was formed (40 minutes). After evaporation in vacuo at 30°-40° C., the residue was dissolved in 25 ml of dry dichloromethane. This solution was dropped into a stirred suspension of 5.72 g (25.0 mmol) of [[[(phenylmethoxy)carbonyl]hydrazino]carbonyl]chloride at 5° C. After stirring for 1 hour at 0° C., the mixture was evaporated in vacuo and the oily residue was stirred with ether containing 4 ml of methanol until it became crystalline; yield after washing with ether and drying in vacuo: 8.77 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04801705 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-b84e99adb2f94653bc0752ecb32eec84 |
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| Source note | uspto-grants-1989_01 |
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