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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184345Generated: November 3, 2026

Carbamic acid, ethyl ester → HCID 86690137, compound

https://huagongshe.com/reaction/1184345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbamic acid, ethyl esterHCID 5641—
ReactantThiophosgeneHCID 10040—
ReactantSodium BicarbonateHCID 516892—
Reactant6-amino-2,2,7-trifluoro-4-(prop-2-ynyl)-2H-benzo[b][1,4]oxazin-3(4H)-oneHCID 86669537—
SolventEthanolHCID 702—
ProductHCID 86690137HCID 8669013790%

Reaction Steps

Sodium bicarbonate (4.10 g, 48.8 mmol) was added to a stirred solution of 6-amino-2,2,7-trifluoro-4-(prop-2-ynyl)-2H-benzo[b][1,4]oxazin-3(4H)-one (the product of Step 1.6 above, 5.0 g, 19.52 mmol) in absolute ethanol (100 ml) at 0° C. under nitrogen. Thereafter thiophosgene (1.795 ml, 23.42 mmol) was added dropwise under ice-bath cooling, keeping the temperature of the reaction mixture below 10° C. After the addition was complete, the reaction mixture was stirred for 1 h at room temperature, by which time, according to TLC analysis, the reaction was complete. The salts were removed by filtration and washed with ethyl acetate. The filtrate was concentrated in vacuo to yield 6.55 g of crude product, containing ca. 30% ethyl carbamate. Recrystallisation from dichloromethane afforded 3.84 g of the desired product (>90% purity), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669208B2
Source datasetuspto-grants-2014_03
ORD IDord-ef8f05c3cbbb4c6991df861781fae432
Source noteuspto-grants-2014_03