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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400776Generated: November 1, 2026

Triphenylphosphine → 5-bromo-2'-chloro-2-methyl-6'-((S)-pent-4-en-2-yloxy)-1,1'-biphenyl

https://huagongshe.com/reaction/1400776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant(2R)-pent-4-en-2-olHCID 6999724—
Reactant5'-Bromo-6-chloro-2'-methyl-[1,1'-biphenyl]-2-olHCID 86710828—
SolventTetrahydrofuranHCID 8028—
Product5-bromo-2'-chloro-2-methyl-6'-((S)-pent-4-en-2-yloxy)-1,1'-biphenylHCID 8671082952.7%

Reaction Steps

5′-Bromo-6-chloro-2′-methyl-[1,1′-biphenyl]-2-ol (540 mg, 1.82 mmol, 1.0 equiv) were mixed with (R)-pent-4-en-2-ol (313 mg, 3.63 mmol, 2.0 equiv) and Ph3P (952 mg, 3.63 mmol, 2.0 equiv) in THF (6 ml). To this solution was added DEAD (1653 μl, 3.63 mmol, 2.0 equiv) dropwise and stirred overnight. The solution was mixed with silica gel and concentrated and purified by 40 g ISCO column with 0-10% EtOAc/hex to afford 5-bromo-2′-chloro-2-methyl-6′-((S)-pent-4-en-2-yloxy)-1,1′-biphenyl (350 mg, 52.7%). 1H NMR (400 MHz, CDCl3) δ 7.39 (dd, J=8.2, 2.1 Hz, 1H), 7.25-7.21 (m, 2H), 7.14 (d, J=7.5 Hz, 1H), 7.07 (d, J=8.0 Hz, 1H), 6.86 (dd, J=8.0, 5.3 Hz, 1H), 5.66-5.50 (m, 1H), 5.05-4.90 (m, 2H), 4.35-4.24 (m, 1H), 2.30-2.12 (m, 2H), 2.01 (s, 3H), 1.16 (dd, J=11.0, 6.0 Hz, 3H). LCMS (M+1)=365.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906929B2
Source datasetuspto-grants-2014_12
ORD IDord-4e81f14299574c2797ff3278128d5cdf
Source noteuspto-grants-2014_12