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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285287Generated: October 26, 2026

Trichlorofluoromethane → Agn-PC-0nfb2Y

https://huagongshe.com/reaction/1285287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichlorofluoromethaneHCID 6389—
ReactantChlorotrifluoroethyleneHCID 6594—
ReactantDichlorodifluoroetheneHCID 11736—
SolventCarbon TetrachlorideHCID 5943—
ProductAgn-PC-0nfb2YHCID 11065502—

Reaction Steps

a process wherein trichlorofluoromethane is added to 1,2-dichlorodifluoroethylene or carbon tetrachloride is added to chlorotrifluoroethylene to obtain 1,1,2-trifluoropentachloropropane, which is then oxidized and esterified to form a 2,3-dichlorotrifluoropropionic acid ester, followed by dechlorination of the ester; (2) a process wherein bromine is added to chlorotrifluoroethylene to obtain 1,2-dibromo-1-chlorotrifluoroethylene, which is then subjected to an addition reaction with propylene, followed by dehydrobromination to obtain 5-bromo-4-chloro-4,5,5-trifluoropentene-2 (CF2BrCFClCH=CHCH3), which is then oxidized and esterified to form a 3-bromo-2-chlorotrifluoropropionic acid ester, which is in turn dehalogenated; and (3) a process wherein chlorotrifluoroethylene is subjected to an addition reaction with hydrogen bromide, followed by dehalogenation to obtain trifluoroethylene, which is then subjected to an addition reaction with ICl, followed by dehydrochlorination to obtain trifluoroiodoethylene, which is then reacted with metallic magnesium in ether to form an organomagnesium intermediate, which is in turn reacted with carbon dioxide, followed by hydrolysis to obtain perfluoroacrylic acid, which is then esterified.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04567003
Source datasetuspto-grants-1986_01
ORD IDord-eef21d5b2b2847aa8d4951b0fe7b9bcf
Source noteuspto-grants-1986_01