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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379942Generated: October 31, 2026

Dibromomethane → HCID 22908410, compound

https://huagongshe.com/reaction/1379942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibromomethaneHCID 3024—
ReactantHexaneHCID 8058—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22908400HCID 22908400—
CatalystZincHCID 23994—
CatalystTitanium TetrachlorideHCID 24193—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22908410HCID 2290841061%

Reaction Steps

A suspension prepared by suspending 3.7 g of zinc dust in 30 ml of tetrahydrofuran was mixed with 1.4 ml of dibromomethane in an atmosphere of argon at a temperature of -20° to -10° C. After stirring for fifteen minutes, 12.5 ml of a dichloromethane solution of 1M titanium tetrachloride was added dropwise to the suspension and stirred at the above temperatures for thirty minutes and at 4° C. for three days. A solution prepared by dissolving 3.33 g of (RS)-3-(1-methyl-2-propenyl)-4-oxocyclopent-2-en-1-yl t-butyldimethylsilyl ether in 15 ml of dichloromethane was added dropwise to the reaction solution in an atmosphere of argon at a temperature of -20° to -10° C. After stirring at an ambient temperature for six hours, 30 ml of hexane was further added to the reaction solution. Under stirring, a suspension prepared by suspending 15 g of sodium hydrogencarbonate in 100 ml of water was added gradually to the reaction solution. After stirring at an ambient temperature for two hours, the reaction solution was filtered through celite, extracted with hexane, and dried over anhydrous magnesium sulfate. After removal of the solvent under reduced pressure, the obtained oily substance was subjected to silica gel column chromatography to yield 2.02 g of (RS)-3-(1-methyl-2-propenyl)-4-methylidenecyclopent-2-en-1-yl t-butyldimethylsilyl ether. Yield 61%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05672779
Source datasetuspto-grants-1997_09
ORD IDord-38c3d12f63d044ee9e180c3a84a4dc56
Source noteuspto-grants-1997_09