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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781535Generated: October 25, 2026

Triphenylphosphine → (E)-4-(1,3-dihydro-6-methoxy-4-methoxyethoxymethoxy-7-methyl-3-oxoisobenzofuran-5-yl)-2-methylbut-2-enyl bromide

https://huagongshe.com/reaction/1781535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
Reactant(E)-4-(1,3-dihydro-6-methoxy-4-methoxyethoxymethoxy-7-methyl-3-oxoisobenzofuran-5-yl)-2-methylbut-2-en-1-olHCID 70303929—
SolventDichloromethaneHCID 6344—
Product(E)-4-(1,3-dihydro-6-methoxy-4-methoxyethoxymethoxy-7-methyl-3-oxoisobenzofuran-5-yl)-2-methylbut-2-enyl bromideHCID 67019128—

Reaction Steps

To a solution of (E)-4-(1,3-dihydro-6-methoxy-4-methoxyethoxymethoxy-7-methyl-3-oxoisobenzofuran-5-yl)-2-methylbut-2-en-1-ol (4.6 g) in methylene chloride (100 ml) at 0° C. was added triphenylphosphine (3.64 g) then N-bromosuccinimide (2.48 g). After 15 minutes the solution was washed with 10% aqueous sodium bisulphite, water, aqueous sodium bicarbonate, then dried and evaporated. The residue was chromatographed on silica gel, eluting with 4:1 hexane: ethyl acetate, to give (E)-4-(1,3-dihydro-6-methoxy-4-methoxyethoxymethoxy-7-methyl-3-oxoisobenzofuran-5-yl) -2-methylbut-2-enyl bromide, mp 74°-75° C. (hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633279
Source datasetuspto-grants-1997_05
ORD IDord-3d832c1fcf3c483f83810b22f9dee1dd
Source noteuspto-grants-1997_05