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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271386Generated: November 1, 2026

HCID 59350344, compound → HCID 46216724, compound

https://huagongshe.com/reaction/2271386

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59350344HCID 59350344—
SolventDichloromethaneHCID 6344—
SolventBoron tribromideHCID 25134—
ProductHCID 46216724HCID 4621672465%

Reaction Steps

To a 0° C. solution of N-(3,4-dimethoxyphenylsulfonyl)-N-hexyl-3,4-dimethoxybenzenesulfonamide (0.080 g, 0.181 mmol) in 1.81 mL of CH2Cl2, boron tribromide (1.81 mL, 1M in CH2Cl2) was added dropwise under a nitrogen atmosphere. The resulting solution was allowed to stir overnight and warm to room temperature. Upon quenching with a few drops of water, a precipitate formed and was filtered. The solid was triturated with ethyl acetate and the filtrate was evaporated, affording 0.046 g (65%) of N-(3,4-dihydroxyphenylsulfonyl)-N-hexyl-3,4-dihydroxybenzenesulfonamide as white solid. 1H NMR (acetone-d6, 400 MHz) δ 7.43 (d, J=2.3 Hz, 2H), 7.34 (dd, J=2.3, 8.2 Hz, 2H), 6.97 (d, J=8.2 Hz, 2H), 3.58 (m, 2H), 1.61 (m, 2H), 1.22 (m, 6H), 0.81 (t, J=6.9 Hz, 3H); 13C NMR (acetone-d6, 100 MHz) δ 150.61, 145.17, 131.03, 121.33, 115.07, 115.06, 49.01, 31.10, 26.05, 22.30, 13.42; HRMS, ES calcd. for C18H23NO8S2Na[M+Na]+468.0763, found: 468.0755.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120744B2
Source datasetuspto-grants-2015_09
ORD IDord-208806a972124685b6fb24d78da84de7
Source noteuspto-grants-2015_09