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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449340Generated: October 30, 2026

Pyridine → Butanedioic acid;bis(2-hydroxy-1,2-diphenylethanone)

https://huagongshe.com/reaction/1449340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSuccinic anhydrideHCID 7922—
ReactantBenzoinHCID 8400—
SolventDimethylformamideHCID 6228—
ProductButanedioic acid;bis(2-hydroxy-1,2-diphenylethanone)HCID 131711721—

Reaction Steps

A clean dry reactor of 20 gallon capacity (91 liters) was charged with pyridine (7.0 kg.) followed by dimethylformamide (35.5 kg.). With agitation, benzoin (18.80 kg.) and succinic anhydride (16.0 kg.) were added. The reactor was flushed with nitrogen. Under a continuing atmosphere of nitrogen, the mixture was heated to 90°-95° C. and maintained within this temperature range for 2 hours. The reaction mixture was cooled to 35°-40° C. After twenty minutes, the reaction mixture was tranferred gradually over 5 hours to a mixture of water (190 kg.) and hydrochloric acid of specific gravity 1.18 (28 kg.) at 55°-60° C. in a reactor of 50 gallon capacity (227 liters). The temperature was maintained at 50°-60° C. over the 5 hour period. Dimethylformamide (9.0 kg.) was used for washing through. The mixture was cooled slowly until product crystallised and then to 15° to 20° C. The mixture was stirred overnight at 15° to 20° C. The product was filtered on a ceramic filter and sucked well dry. The product was then washed with water ten times with 20 kg. each time. Ater each wash portion the product was sucked well dry. The product was then dried in a circulating air oven at 50°-60° C. for 12 to 18 hours. The yield obtained was 25.5 kg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04190584
Source datasetuspto-grants-1980_02
ORD IDord-5c05009bde3b4ca3bb3643e3205269ff
Source noteuspto-grants-1980_02