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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155666Generated: November 1, 2026

Water → 3-Phenoxybenzyl (1S,3R)-3-(2-chloro-3,3,3-trifluoro-1-propen-1-yl)-2,2-dimethylcyclopropanecarboxylate-rel-

https://huagongshe.com/reaction/1155666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
Reactant3-Phenoxybenzyl alcoholHCID 26295—
Reactanttrans-3-[2-Chloro-3,3,3-trifluoropropenyl]-2,2-dimethylcyclopropanecarbonyl chlorideHCID 86736786—
SolventDichloromethaneHCID 6344—
Product3-Phenoxybenzyl (1S,3R)-3-(2-chloro-3,3,3-trifluoro-1-propen-1-yl)-2,2-dimethylcyclopropanecarboxylate-rel-HCID 156450—

Reaction Steps

To a stirred solution of 1.8 g (0.007 mole) of trans-3-[2-chloro-3,3,3-trifluoropropenyl]-2,2-dimethylcyclopropanecarbonyl chloride in 10 ml of methylene chloride at ambient temperature was added a solution of 1.6 g (0.008 mole) of 3-phenoxybenzyl alcohol and 0.73 g (0.009 mole) of pyridine in 5 ml of methylene chloride. Upon complete addition the reaction mixture was stirred at ambient temperature for 3 hours, then poured into 50 ml of water. The organic layer was separated, and the aqueous layer was extracted with three portions of 50 ml each of methylene chloride. The combined extracts were dried with sodium sulfate, filtered, and the filtrate evaporated under reduced pressure to a residual oil. Volatile components were removed from the oil at 125° C./0.05 mm using a Kugelrohr distillation system. The pot residue was 99% 3-phenoxybenzyl trans-3-[2-chloro-3,3,3-trifluoropropenyl]-2,2-dimethylcyclopropanecarboxylate, as determined by gas chromatographic analysis. The weight of product was 2.0 g. The nmr and ir spectra were consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04332815
Source datasetuspto-grants-1982_06
ORD IDord-a3c76d51fe714e99927e906a8131e5fb
Source noteuspto-grants-1982_06