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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437599Generated: November 1, 2026

Phosphoric Acid → (Z)-4-Acetoxy-3-(4-(methylsulfonyl) phenyl)-2-phenylbut-2-enoic acid

https://huagongshe.com/reaction/1437599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
Reactant2-Methyl-2-buteneHCID 10553—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantSodium ChloriteHCID 23668197—
Reactant(2Z)-4-hydroxy-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-enyl acetateHCID 58787789—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
Product(Z)-4-Acetoxy-3-(4-(methylsulfonyl) phenyl)-2-phenylbut-2-enoic acidHCID 1161771693%

Reaction Steps

To a solution of 38.3 g of (2Z)-4-hydroxy-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-enyl acetate in 500 mL of dichloromethane, 47 g of Dess-Martin reagent was added and the resulted mixture was stirred at rt for 2 h. Then 2 mL of water was added and the resulted mixture was stirred at rt for 1 h. Then the mixture was filtered and evaporated. The crude thus obtained was dissolved in a solvent mixture of 200 mL of THF with 200 mL of t-BuOH. To the resulted mixture, 30 mL of 2-methyl-2-butene was added and followed by the addition of 200 mL of 1.2 M of phosphoric acid and 200 mL of 1 M of NaClO2. The resulting mixture was stirred at rt for 30 nm in. The organic phase was separated and the aqueous phase was extracted with EtOAc. The organic phase was combined, dried over Na2SO4, filtered, and then evaporated. The crude was purified by recrystallization from ether to afford 37 g of the titled compound as white solids 1H NMR (acetone-d6, 500 MHz): δ 7.76 (d, 2H), 7.43 (d, 2H), 7.18-7.12 (m, 3H), 7.12-7.08 (m, 2H), 5.24 (s, 2H), 3.05 (s, 3H), 1.88 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622502B2
Source datasetuspto-grants-2009_11
ORD IDord-bf32333e144d44e49454aa2405b3ad55
Source noteuspto-grants-2009_11