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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898764Generated: October 30, 2026

Tetrahydrofuran → Methyl 5-Acetoxy-2-bromomethyl-4-methoxyhydrocinnamate

https://huagongshe.com/reaction/1898764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantMethyl 5-Hydroxy-2-tert-butyldimethylsilyloxymethyl-4-methoxyhydrocinnamateHCID 23372374—
SolventDiethyl EtherHCID 3283—
ProductMethyl 5-Acetoxy-2-bromomethyl-4-methoxyhydrocinnamateHCID 23372383—

Reaction Steps

To a solution of methyl 5-hydroxy-2-tert-butyldimethylsilyloxymethyl-4-methoxyhydrocinnamate (5.21 g) in carbon tetrabromide (12.35 g) in anhydrous ether (75 ml) and anhydrous THF (50 ml) is added portionwise triphenylphosphine (9.78 g) and the mixture stirred at room temperature for 60 minutes, diluted with ether, then filtered. The filtrate is concentrated in vacuo and the residue purified by filtration through silica gel in 50% ethyl acetate in hexanes followed by HPLC, eluting with 25% ethyl acetate in hexanes, to give the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571506
Source datasetuspto-grants-1996_11
ORD IDord-94763bb1c83c48a3b83869585f59d137
Source noteuspto-grants-1996_11