Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607358Generated: October 25, 2026

Water → HCID 13602242, compound

https://huagongshe.com/reaction/1607358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetic AnhydrideHCID 7918—
Reactant1,1,1-Trichloro-2,2,2-trifluoroethaneHCID 9635—
ReactantMethyl 3-formyl-2,2-dimethylcyclopropanecarboxylateHCID 3016263—
CatalystZincHCID 23994—
SolventDimethylformamideHCID 6228—
ProductHCID 13602242HCID 1360224243%
ProductHCID 13956728HCID 1395672835%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 156 mg (1.00 mmol) of methyl 2,2-dimethyl-3-formylcyclopropanecarboxylate in 1 ml of DMF, 78 mg (1.19 mmol) of zinc powder and 0.177 ml (1.50 mmol) of 1,1,1-trichlorotrifluoroethane were added at 0° C., and the mixture was stirred at 0° C. for 30 minutes and at 50° C. for 10 hours. Then, 0.5 ml of acetic anhydride was added at room temperature, and the mixture was stirred for 10 minutes. After an addition of 2 ml of water, the mixture was extracted with diethyl ether (2 ml×5 times). The extract was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to obtain a crude product. The crude product was purified by thin layer chromatography (silica gel, dichloromethane/hexane=2/3) to isolate 122 mg (35%) of methyl 2,2-dimethyl-3-(1-acetoxy-2,2-dichloro-3,3,3-trifluoropropyl)cyclopropanecarboxylate and 133 mg (43%) of methyl 2,2-dimethyl-3-(1-hydroxy-2,2-dichloro-3,3,3-trifluoropropyl)cyclopropanecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04864052
Source datasetuspto-grants-1989_09
ORD IDord-e37e8065015d4d629a5fa30dae587d86
Source noteuspto-grants-1989_09