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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895823Generated: November 1, 2026

Butyric anhydride → HCID 86190388, compound

https://huagongshe.com/reaction/1895823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyric anhydrideHCID 7798—
ReactantAcetic AnhydrideHCID 7918—
ReactantSuccinic anhydrideHCID 7922—
ReactantGlutaric anhydrideHCID 7940—
Reactant1,1-Dichloro-1,2,2,2-tetrafluoroethaneHCID 9775—
ReactantPropionic anhydrideHCID 31263—
ReactantAdipic anhydrideHCID 567658—
CatalystZincHCID 23994—
ProductHCID 86190388HCID 86190388—

Reaction Steps

This reaction may be run as described with addition of both reagents in the same reaction vessel or the acid anyhydride may be added alone to produce CF3CClFCH2OC(═O)CH3, which may be isolated. And then the reactive metal may be added to the CF3CClFCH2OC(═O)CH3 to produce the HFO-1234yf. In this process the carboxylic acid anhydride is selected from the group consisting of acetic anhydride, propionic anhydride, butyric anhydride, succinic anhydride, glutaric anhydride, and adipic anhydride. The reactive metal powder is as described previously herein. The reductive dehydroxychlorination can be done without neutralizing the product mixture from the reaction of CFC-114a with zinc and an aldehyde. Or the reductive dehydroxychlorination may be done after first isolating the CF3CClFCH2OH, and then esterification by reaction with a carboxylic acid anhydride and a reactive metal to form CF3CClFCH2OC(═O)CH3. Any of these dehydroxychlorinations produce Composition C as described above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518294B2
Source datasetuspto-grants-2013_08
ORD IDord-f34c0e391c3c493991af422579d1efea
Source noteuspto-grants-2013_08