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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359161Generated: October 31, 2026

Dimethylformamide → HCID 22672848, compound

https://huagongshe.com/reaction/1359161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
ReactantCesiumHCID 5354618—
ReactantHCID 22672852HCID 22672852—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 22672848HCID 22672848—

Reaction Steps

A suspension of the title D compound, 2-benzyloxy-5-(2,6-dimethyl-4-nitrophenoxy)benzenesulfonic acid, cesium salt (9.9 9, 20 mmol) in 200 mL of CH2Cl2 is treated with DMF (3.1 mL, 40 mmol), then oxalyl chloride (3.5 mL, 40 mmol) is added over 30 min at RT. The reaction mixture is stirred for 1 h further, then diluted with Et2O (200 mL) and washed with water and brine, dried over anhydrous sodium sulfate (Na2SO4) and concentrated. The product is washed with Et2O (5 mL) and dried in vacuo to afford 2-benzyloxy-5-(2,6-dimethyl-4-nitrophenoxy)benzenesulfonyl chloride: NMR (CDCl3) 2.24 (s, 6H), 5.31 (s, 2H), 7.02 (dd, 1 H, J=8.7, 3.8), 7.10 (d, 1H, J=8.7), 7.32-7.47 (m, 4H), 7.52 (d, 2H, J=7.5), 8.05 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599942B1
Source datasetuspto-grants-2003_07
ORD IDord-9e2747a0d5d14cbba5829dbfb1503786
Source noteuspto-grants-2003_07