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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542879Generated: October 30, 2026

Succinic anhydride → HCID 20207520, compound

https://huagongshe.com/reaction/542879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSuccinic anhydrideHCID 7922—
ReactantBenzoinHCID 8400—
ReactantAmmonium AcetateHCID 517165—
ReactantHCID 12505004HCID 12505004—
SolventAcetic AcidHCID 176—
SolventTolueneHCID 1140—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 20207520HCID 2020752096.9%

Reaction Steps

4'-Methoxybenzoin (17.4 g, 0.0716 m) prepared according to R. T. Arnold and R. C. Fuson, J.A.C.S., 58, 1295 (1936), succinic anhydride (8.7 g, 0.086 m), triethylamine (3.541, 0.025 m) and toluene (30 ml) were heated on a steam cone under nitrogen for 2.5 hours. Thin layer chromatography (silica gel 60, ethyl acetate) showed complete conversion of the starting benzoin. Glacial acetic acid (40 ml) and ammonium acetate (7.6 g) were added and 40 ml of solvent were removed by distillation over 1 hour. Glacial acetic acid (40 ml) was added and 40 ml solvent removed by distillation. Glacial acetic acid (40 ml) was added and again 40 ml solvent removed by distillation. The cooled mixture was poured into 600 ml of ice water and the solid product was filtered. The product was purified by chromatography on a silica gel column using gradient elution from 100% chloroform to 90% chloroform:10% ethylacetate. Crystallization of the residue (29 g) from 200 ml of 50% aq. methanol gave 22.5 g of 5-(4-methoxyphenyl)-4-phenyl-2-oxazolepropanoic acid, m.p. 123°-126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04659728
Source datasetuspto-grants-1987_04
ORD IDord-acac3c9fc0264459a1a0a00be32cc26c
Source noteuspto-grants-1987_04