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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247918Generated: October 26, 2026

Boron trifluoride etherate → Methyl 3-ethoxy-2-(ethoxyimino)-3-iminopropanoate

https://huagongshe.com/reaction/1247918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantTriethylamineHCID 8471—
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
ReactantMethyl 3-amino-2-(ethoxyimino)-3-oxopropanoateHCID 53690437—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-ethoxy-2-(ethoxyimino)-3-iminopropanoateHCID 53663360—

Reaction Steps

To a solution of Meerwein reagent (triethyloxonium tetrafluoroborate) {prepared from boron fluoride etherate (2.84 g) by a method of Org. Syn., 46, 113 (1966)} in methylene chloride (30 ml) was added methyl 2-carbamoyl-2-ethoxyiminoacetate (syn isomer, 2.6 g) and the mixture was stirred for 18 hours at room temperature. The reaction mixture was cooled in an ice-bath and triethylamine (3 g) was added thereto, followed by an addition of water (20 ml). The organic layer was separated out, dried over magnesium sulfate and evaporated to give crude methyl 3-imino-3-ethoxy-2-ethoxyiminopropionate (syn isomer) (5.0 g) as an oil. ##STR14##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04521413
Source datasetuspto-grants-1985_06
ORD IDord-ce94f06b2c1b4a598fdad22af5a00bbe
Source noteuspto-grants-1985_06