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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589580Generated: October 30, 2026

Methanol → HCID 59818345, compound

https://huagongshe.com/reaction/589580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfamic AcidHCID 5987—
ReactantSodium ChloriteHCID 23668197—
Reactant4′-Fluoro-2′-methoxy-5′-(1-methylethyl)-4-(trifluoromethyl)[1,1′-biphenyl]-2-carboxaldehydeHCID 59135225—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59818345HCID 59818345—

Reaction Steps

An 8.2 g quantity of a mixture of 4′-fluoro-5′-isopropyl-2′-methoxy-4-(trifluoromethyl)biphenyl-2-yl)methanol 16b and 4′-fluoro-5′-isopropyl-2′-methoxy-4-(trifluoromethyl)biphenyl-2-carbaldehyde 56 [obtained, as a mixture, from a Suzuki coupling by methods described in WO2007/005572] was dissolved along with sulfamic acid (3.3 g) in a mixture of THF (50 mL) and water (50 mL) The solution was cooled in an ice bath. A solution of 80% NaClO2 (2.6 g) in water (50 mL) was added dropwise from an addition funnel. When addition was complete, the mixture was stirred at <8° C. for 1.5 hr. The mixture was quenched by addition of water and extracted with EtOAc. The organic phase was concentrated under reduced pressure to a volume of ˜50 mL and extracted with 2N KOH (20 mL×2). The organic phase was reserved. The aqueous solution was acidified to pH 2, and the solid filtered, to yield 300-400 mg of product 57 as a first crop. The reserved organic solution was concentrated under reduced pressure and the resulting crude product purified by chromatography on silica gel to give a total of 1.4-1.5 g of 57.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233938B2
Source datasetuspto-grants-2016_01
ORD IDord-ebbe6744e3004f92876e950a670d6728
Source noteuspto-grants-2016_01