Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873729Generated: October 30, 2026

Ethyl bromodifluoroacetate → HCID 86724272, compound

https://huagongshe.com/reaction/873729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromodifluoroacetateHCID 69585—
ReactantHCID 86724254HCID 86724254—
CatalystZincHCID 23994—
SolventEther tetrahydrofuranHCID 21868444—
ProductHCID 86724272HCID 8672427296.6%

Reaction Steps

To a suspension of activated zinc (3.44 g, 52.5 mmol) in Et2O-THF (50% v/v, 80 ml) under reflux was slowly added a solution of ethyl bromodifluoroacetate (8.00 g, 39.4 mmol) and N-(6-bromo-4H-spiro[chromene-3,1′-cyclopropan]-4-ylidene)-2-methylpropane-2-sulfinamide (4.68 g, 13.1 mmol) in Et2O-THF (50% v/v, 80 ml) over 40 minutes, and the mixture was stirred for 4 hours at the same temperature. After cooling, the mixture was filtrated through celite pad and washed with EtOAc. To the filtrate were added saturated aqueous NH4Cl and EtOAc. After separation, the water layer was extracted with EtOAc. The combined organic layer was dried over MgSO4 and concentrated. The residue was purified by silica gel chromatography (EtOAc:hexane=20:80-100:0) to give ethyl {6-bromo-4-[(tert-butylsulfinyl)amino]-4H-spiro[chromene-3,1′-cyclopropan]-4-yl}(difluoro)acetate (6.08 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975415B2
Source datasetuspto-grants-2015_03
ORD IDord-8acaf54feea44618b518382a3c4ec08b
Source noteuspto-grants-2015_03