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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170975Generated: November 1, 2026

Carbon tetrabromide → HCID 25150222, compound

https://huagongshe.com/reaction/1170975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 11131640HCID 11131640—
SolventDiethyl EtherHCID 3283—
ProductHCID 25150222HCID 2515022254.2%

Reaction Steps

To a stirred solution of triphenylphosphine (0.42 g, 1.61 mmol) and CBr4 (0.534 g, 1.61 mmol) in diethyl ether (15.0 mL) at room temperature was added 4-(3′-iso-propyl-4′-methoxyphenoxy)-3,5-dichlorobenzyl alcohol (0.50 g, 1.46 mmol). The reaction mixture was stirred at room temperature for 16 h, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel, eluting with acetone-hexanes (1:9) to afford 3,5-dichloro-4-(3′-iso-propyl-4′-methoxyphenoxy)benzyl bromide (0.320 g, 54%): 1H NMR (300 MHz, DMSO-d6): δ 7.77 (s, 2 H), 6.82 (m, 2 H), 6.38 (m, 1 H), 4.75 (s, 2 H), 3.75 (s, 3 H), 3.22 (m, 1 H), 1.13 (d, J=6.0 Hz, 6 H); TLC conditions: Uniplate silica gel, 250 microns; Mobile phase=hexanes-acetone (1:4); Rf=0.46.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829552B2
Source datasetuspto-grants-2010_11
ORD IDord-082763e2dfdc422595f0c9560be70ab3
Source noteuspto-grants-2010_11