Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192888Generated: October 25, 2026

Hydrochloric Acid → HCID 68671827, compound

https://huagongshe.com/reaction/2192888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriphenyl[(tetrahydro-2H-pyran-4-yl)methyl]phosphonium iodideHCID 21094223—
ReactantEthyl [3-bromo-4-(cyclopropylsulfanyl)phenyl](oxo)acetateHCID 59570898—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68671827HCID 6867182773.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of triphenyl(tetrahydro-2H-pyran-4-yl-methyl)phosphonium iodide (9.27 g) in THF (70 mL) was added dropwise lithium-1,1,1,3,3,3-hexamethyldisilazide (1 M THF solution, 19.0 mL) at 0° C. or lower, followed by stirring at around 0° C. for 1 hour. To the reaction mixture was added dropwise a solution of ethyl[3-bromo-4-(cyclopropylsulfanyl)phenyl](oxo)acetate (5.0 g) in THF (10 mL) at 2° C. or lower. The reaction mixture was stirred for 30 minutes under ice-cooling and then stirred at room temperature for 15 hours. 4 M Hydrochloric acid was added dropwise thereto at 10° C. or lower, adjusted to pH 7, and then concentrated under reduced pressure. To the residue was added diethyl ether and the resulting solid was separated by filtration. The filtrate was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain ethyl 2-[3-bromo-4-(cyclopropylsulfanyl)phenyl]-3-(tetrahydro-2H-pyran-4-yl)acrylate (4.57 g) as an (E)/(Z)-mixture of olefin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329707B2
Source datasetuspto-grants-2012_12
ORD IDord-ab831bb4367c4bb3b98bd26cbb64fea6
Source noteuspto-grants-2012_12