Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382772Generated: October 30, 2026

4-Nitrobenzenesulfonyl chloride → HCID 15539132, compound

https://huagongshe.com/reaction/382772

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): δ 2.29 (s, 1 H), 2.84, 3.47 {AB q of d, J=12.4(3.8) Hz, 12.4(7.9) Hz, 4 H}, 3.30 (m, 1 H), 4.46, 5.07 (AB q, J=12.5 Hz, 2 H), 5.31 (s, 1 H), 8.11, 8.41 (AB q, J=8.7 Hz, 8 H); 13C NMR (DMSO-d6): δ 50.0, 59.8, 60.6, 124.6, 128.9, 143.3, 150.1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310204B1
Source datasetuspto-grants-2001_10
ORD IDord-cf69d65206dd47ac8fa37ff1c0b87061
Source noteuspto-grants-2001_10