Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647113Generated: October 24, 2026

Triethylamine → Methyl 3-ethoxy-2-(ethoxyimino)-3-iminopropanoate

https://huagongshe.com/en/reaction/647113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantFluoride IonHCID 28179—
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 bron 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. ##STR15##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04407798
Source datasetuspto-grants-1983_10
ORD IDord-c2c14045175f4522914e930aa28b5372
Source noteuspto-grants-1983_10