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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973872Generated: October 29, 2026

Triphenylphosphine → HCID 67923948, compound

https://huagongshe.com/reaction/973872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 19988399HCID 19988399—
SolventBenzeneHCID 241—
ProductHCID 67923948HCID 67923948—

Reaction Steps

5-Bromo-2,5-dihydro-4-methoxy-3-methyl-2-oxofuran (6.44 g) was dissolved in dry benzene (100 mls). Triphenylphosphine was added and the solution stirred overnight at room temperature. The solution was decanted from the orange gum, which was then triturated with ether to give a colourless crystalline solid. The ether was decanted and the salt dried under vacuum. The decanted solution was concentrated to a gum. Trituration of this with ether resulted in a second crop of the phosphonium salt. The combined crops gave the title compound as a colourless solid, (14 41 g, 99%), νmax (CH2Cl2) 1775, 1665, 1435, 1390 and 1330cm-1 ; δH (CDCl3) 1.74 (3H, m), 3.95 (3H, s) and 7.5-8.1 (16H, m); [mass spectrum: +ve ion (3NOBA, Na+) M+ -Br, 389].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05064649
Source datasetuspto-grants-1991_11
ORD IDord-4dc41db48a714890bac65186905ab619
Source noteuspto-grants-1991_11