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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937737Generated: November 2, 2026

4-Nitrobenzenesulfonyl chloride → HCID 15539132, compound

https://huagongshe.com/reaction/1937737

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzenesulfonyl chlorideHCID 7404—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 10953438HCID 10953438—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 15539132HCID 1553913295%

Reaction Steps

A solution of hexahydro-5-pyrimidinol (1.0 g, 9.8 mmol) and sodium carbonate (1.04 g, 9.8 mmol) in 10 mL of water in a 250 mL round bottom flask was stirred with a magnetic stir bar for 10 minutes. A solution of 4-nitrobenzenesulfonyl chloride (4.4 g, 19.8 mmol) in 10 mL of toluene was added dropwise over a period of 30 minutes. The reaction mixture formed a white suspended solid. A mixture of 100 mL of water and 20 mL of toluene was added to the reaction mixture and stirred overnight. The reaction mixture was filtered and the solid was washed with 100 mL of toluene, then with 100 mL of water. The solid was dried at room temperature under reduced pressure to give 4.4 g (95%) of crude product, hexahydro-1,3-bis(4-nitrobenzenesulfonyl)-5-pyrimidinol. [1H NMR (DMSO-d6): δ2.29 (s, 1H), 2.84, 3.47 {AB q of d, J=12.4(3.8) Hz, 12.4(7.9) Hz, 4H}, 3.30 (m, 1H), 4.46, 5.07 (AB q, J=12.5 Hz, 2H), 5.31 (s, 1H), 8.11, 8.41 (AB q, J=8.7 Hz, 8H); 13C NMR (DMSO-d6): δ50.0, 59.8, 60.6, 124.6, 128.9, 143.3, 150.1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395899B2
Source datasetuspto-grants-2002_05
ORD IDord-5cfe5c34ae3c4abfbb12c94acb1e79de
Source noteuspto-grants-2002_05