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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108615Generated: October 30, 2026

Carbon tetrabromide → HCID 25150222, compound

https://huagongshe.com/reaction/2108615

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)benzylbromide (0.320 g, 54%): 1H NMR (300 MHz, DMSO-d6): δ 7.77 (s, 2H), 6.82 (m, 2H), 6.38 (m, 1H), 4.75 (s, 2H), 3.75 (s, 3H), 3.22 (m, 1H), 1.13 (d, J=6.0 Hz, 6H); 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 numberUS07514419B2
Source datasetuspto-grants-2009_04
ORD IDord-00d32623b6704a56b933d0698aa1772b
Source noteuspto-grants-2009_04