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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292344Generated: October 31, 2026

Methanol → HCID 14390900, compound

https://huagongshe.com/reaction/2292344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN-methyl-N-(trimethylsilyl)trifluoroacetamideHCID 32510—
ReactantHCID 21277172HCID 21277172—
ReactantPhenylmethyl 2-(chlorocarbonyl)hydrazinecarboxylateHCID 21681927—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 14390900HCID 14390900—

Reaction Steps

15.64 ml (80.0 mmol) of N-methyl-N-trimethylsilyltrifluoroacetamide was added to a suspension of 4.80 g (20.0 mmol) of 4-aminocatechol trifluoroacetate in 80 ml of dry acetonitrile. After stirring for 30 minutes, the dark solution was evaporated in vacuo and the dark residue was redissolved in 25 ml of dichloromethane. A solution of 4.56 g (20.0 mmol) of 2-(chlorocarbonyl)hydrazinecarboxylic acid, phenylmethyl ester in 50 ml of dichloromethane was slowly dropped in with stirring at 10° C. (40 minutes), and stirring was continued for 2 hours at room temperature. After evaporation in vacuo, the residue was taken up in a few ml of methanol and stirred until it became crystalline. The suspension was dluted with ether, and the precipitate was collected by suction; yield: 6.09 g, melting point 204° C., dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04801705
Source datasetuspto-grants-1989_01
ORD IDord-6a8d4420ff5f4659a7a166e260f9cc95
Source noteuspto-grants-1989_01