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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069979Generated: October 25, 2026

N-acetyl-N'-tert-butyl-5-formyl-6-methoxy-biphenyl-3,3'-disulfonamide → HCID 86607737, compound

https://huagongshe.com/reaction/2069979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-acetyl-N'-tert-butyl-5-formyl-6-methoxy-biphenyl-3,3'-disulfonamideHCID 86607706—
SolventDichloromethaneHCID 6344—
ProductHCID 86607737HCID 8660773788.4%

Reaction Steps

N-acetyl-N′-tert-butyl-5-formyl-6-methoxy-biphenyl-3,3′-disulfonamide (100 mg, 0.21 mmol), prepared as in Reference 19, was dissolved in dichloromethane (10 mL). The solution was flushed with nitrogen for 5 minutes and then boron tribromide (1.0 mL, 1M solution in dichloromethane) was added. The mixture was stirred at room temperature for 1 hour and then concentrated under by evaporation under reduced pressure. The residue was partitioned between water and ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The residue was passed through a short silica plug with pure ethyl acetate to give N-acetyl 5-formyl-6-hydroxy-biphenyl-3,3′-disulfonamide (74 mg) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299110B2
Source datasetuspto-grants-2012_10
ORD IDord-140a0da882bf44e7be3f365ecc8490c0
Source noteuspto-grants-2012_10