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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-N-(trimethylsilyl)trifluoroacetamideHCID 32510—
Reactant3,4-DihydroxybenzohydrazideHCID 586300—
ReactantPhenylmethyl 2-(chlorocarbonyl)hydrazinecarboxylateHCID 21681927—
SolventAcetonitrileHCID 6342—
ProductHCID 56974509HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04801705
Source datasetuspto-grants-1989_01
ORD IDord-b84e99adb2f94653bc0752ecb32eec84
Source noteuspto-grants-1989_01