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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638310Generated: October 29, 2026

Acetic Acid → HCID 12795037, compound

https://huagongshe.com/reaction/638310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 1-(2-acetoxyethyl)-4-bromopyrrole-2-glyoxalateHCID 12795028—
SolventMethanolHCID 887—
ProductHCID 12795037HCID 12795037—

Reaction Conditions

Temperature-50 °C

Reaction Steps

Methanol (100 ml) containing 2.5 ml water is cooled to -50° C. and 3.07 g of sodium borohydride (81.2 mmole) is added with stirring. After 5 minutes, ethyl 1-(2-acetoxyethyl)-4-bromopyrrole-2-glyoxalate (8.9 g -26.7 mmole) is dissolved in 40 ml methanol and added at a rate such that the reaction temperature does not exceed -40° C. After 1 hour at this temperature, 50% aqueous acetic acid is added until the solution is weakly acidic. The methanol is then removed in vacuo, 100 ml ethyl acetate is added to the residue, and the organic phase is washed well with saturated salt solution and then dried over sodium sulfate. The solvent is removed in vacuo and the residue is immediately crystallized, at low temperature (dry ice-acetone bath), from ether. The ethyl 1-(2-acetoxyethyl)-4-bromopyrrole-2-glycolate thus obtained (6.0 g, 67%) exhibits a m.p. of 59° C. but is unstable and is be stored in an evacuated vessel at -10° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04560699
Source datasetuspto-grants-1985_12
ORD IDord-5967890fffa64e67b03dd4d478cf6d28
Source noteuspto-grants-1985_12