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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622159Generated: October 25, 2026

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

https://huagongshe.com/reaction/1622159

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 numberUS08778625B2
Source datasetuspto-grants-2014_07
ORD IDord-68ed2e6906b0475797b1b7b88b7c15f3
Source noteuspto-grants-2014_07