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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581659Generated: November 1, 2026

Acetic acid, azido-, ethyl ester → HCID 72644371, compound

https://huagongshe.com/reaction/1581659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, azido-, ethyl esterHCID 69480—
ReactantSodiumHCID 5360545—
ReactantHCID 12962657HCID 12962657—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 72644371HCID 7264437155.1%

Reaction Conditions

Temperature-15 °C

Reaction Steps

Sodium (20.0 g, 0.870 mol) was dissolved in absolute ethanol (550 mL) and the resulting solution cooled to −15° C. A mixture of 4-methoxy-3-thiophenaldehyde (32.4 g, 0.228 mol) and ethyl azidoacetate (118 g, 0.914 mol) in absolute ethanol (30 mL) and ether (30 mL) was added slowly such that the temperature of the reaction mixture did not rise above −10° C. The mixture warmed to −40° C. over 40 min accompanied by vigorous gas evolution. After 3 h the mixture was diluted with water (1 L) and the resulting precipitate was collected via vacuum filtration to provide 31.8 g (55%) of the title compound. Recrystallization (hexanes) of an analytical sample provided yellow crystals: mp 88-90° C. 1H NMR (CDCl3) 88.14 (d, J=3.3 Hz, 1H), 6.94 (s, 1H), 6.19 (d, J=3.3 Hz, 1H), 4.35 (q, J=7.0 Hz, 2H), 3.86 (s, 3H), 1.41 (t, J=7.0 Hz, 3H); MS ES+m/e 254 (p+1); IR (KBr, cm−1) 2114, 1700, 1256. Anal. Calcd for C10H11N3O3S: C, 47.42; H, 4.38; N, 16.59. Found: C, 47.09; H, 4.46; N, 15.87.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730694B1
Source datasetuspto-grants-2004_05
ORD IDord-5c07cdba83ba47dd88d36ed5249a35e7
Source noteuspto-grants-2004_05