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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354647Generated: November 1, 2026

Trityl chloride → HCID 4081485, compound

https://huagongshe.com/reaction/354647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
ReactantEthyl 2-(2-aminothiazol-4-yl)-2-methoxyiminoacetateHCID 581091—
SolventDichloromethaneHCID 6344—
ProductHCID 4081485HCID 408148565%

Reaction Conditions

Temperature-35 °C

Reaction Steps

2.9 ml of triethylamine were added at -10° C. to a mixture of 4.6 g of the product of Step A in 92 ml of methylene chloride and after cooling to -35° C., 6.1 g of trityl chloride were added thereto. The temperature was allowed to rise to room temperature in about 21/2 hours and the reaction mixture was washed with water and then with 0.5 N hydrochloric acid and finally with aqueous sodium acetate. The mixture was dried and evaporated to dryness. The residue was taken up in ether and the solution was concentrated to dryness again. The residue was dissolved in methanol and water and ether were added to cause crystallization. The mixture was vacuum filtered and the recovered precipitate was washed with ether to obtain 6.15 g of ethyl 2-(2-tritylamino-4-thiazolyl)-2-methoxyiminoacetate melting at 120° C. having the syn configuration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04376203
Source datasetuspto-grants-1983_03
ORD IDord-a9a1a43bf8fa4fd4a47c5cb12b7a3b64
Source noteuspto-grants-1983_03