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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427342Generated: October 26, 2026

Sodium Hydroxide → HCID 178465665, compound

https://huagongshe.com/reaction/1427342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactanttert-Butyl carbazateHCID 70091—
ReactantEthanimidic acid, ethyl ester, hydrochloride (1:1)HCID 2724290—
SolventEthanolHCID 702—
ProductHCID 178465665HCID 178465665—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydroxide (16.0 g, 400 mmol) was dissolved in absolute ethanol (1 L) at 60° C. The solution was cooled to 0° C. and treated portion-wise with ethyl ethanimidoate hydrochloride (50 g, 400 mmol); after 10 minutes, tert-butyl hydrazinecarboxylate (52.9 g, 400 mmol) was added in a single portion. The reaction mixture was stirred at 70° C. for 2.5 hours, then cooled to 20° C. and filtered. The filtrate was concentrated in vacuo and treated with tert-butyl methyl ether (500 mL) and ethanol (20 mL). After seeding, the mixture was allowed to stir for 18 hours, whereupon the precipitated solid was collected via filtration and washed with ice-cold tert-butyl methyl ether (500 mL). The solid was dissolved in 2-methyltetrahydrofuran:methanol (9:1 mixture, 300 mL), and the solution was concentrated to dryness. The residue was washed with diethyl ether (3×200 mL) to afford the product as a very pale yellow solid. Yield; 50.2 g, 290 mmol, 72%. LCMS m/z 174.3 [M+H]+. 1H NMR (500 MHz, CD3OD) δ 1.88 (s, 3H), 1.47 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933224B2
Source datasetuspto-grants-2015_01
ORD IDord-c5c4cd0d59a149cb9724ab96065d79d4
Source noteuspto-grants-2015_01