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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064749Generated: October 26, 2026

Sodium Carbonate → 4'-Hydroxy-5'-iodo-3'-methyl-1,1'-biphenyl-4-carbonitrile

https://huagongshe.com/reaction/1064749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantSodium SulfiteHCID 24437—
Reactant1,1,3,3-TetramethylguanidineHCID 66460—
ReactantN-IodosuccinimideHCID 120273—
ReactantMonobasic potassium phosphateHCID 516951—
Reactant4'-Hydroxy-3'-methyl-[1,1'-biphenyl]-4-carbonitrileHCID 22274497—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product4'-Hydroxy-5'-iodo-3'-methyl-1,1'-biphenyl-4-carbonitrileHCID 2227458317%

Reaction Steps

4′-hydroxy-3′-methyl-1,1′-biphenyl-4-carbonitrile (875 mg, 4.18 mmol) was dissolved into DMF (20 mL) and treated with N-iodosuccinimide (1.012 g, 4.5 mmol). The solution was stirred at room temperature for four days. Then the mixture was stirred with tetramethylguanidine (1 mL) for ten minutes, poured into an aqueous mixture of Na2SO3 and Na2CO3, adjusted to pH 9 with aqueous potassium dihydrogen phosphate, and diluted with ether. The gum which separated from the biphasic mixture was dissolved into EtOAc and added to a rapidly stirred mixture of the aqueous phase and ether. The organic phase was separated, filtered, combined with the original ethereal phase, concentrated, and chromatographed through silica with a 50% to 100% gradient of CH2Cl2/hexanes to provide the title compound as an off-white powder (17% yield). MS (ESI APCI negative ion detection) m/z 334 (M−H)−; 1HNMR (300 MHz, CDCl3) δ 2.38 (s, 3 H), 7.26 (s, 1 H), 7.33 (d, 1 H), 7.60 (d, 2 H), 7.66-7.74 (m, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969730B2
Source datasetuspto-grants-2005_11
ORD IDord-99d1f510ff014e67b6ea4abe07c57cb0
Source noteuspto-grants-2005_11