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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585050Generated: October 30, 2026

4-Toluenesulfonyl chloride → HCID 22734543, compound

https://huagongshe.com/reaction/585050

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 22182528HCID 22182528—
SolventDichloromethaneHCID 6344—
ProductHCID 22734543HCID 2273454345.8%

Reaction Steps

(7,8-Dihydro-6H-5-oxa-1-aza-phenanthren-6-yl)-methanol (0.27 g, 1.3 mmole) was dissolved in 75 mL of methylene chloride and p-toluenesulfonyl chloride (0.60 g, 3.1 mmole) added. The mixture was placed in an ice/isopropanol bath and first N,N-diisopropylethylamine (0.55 mL, 3.1 mmole) and then N,N-dimethyaminopyridine added. The mixture was allowed to stir under nitrogen for 5 days. It was washed with 150 mL portions of 2 N aqueous HCl, saturated aqueous sodium bicarbonate and saturated brine, dried over magnesium sulfate, filtered and concentrated in vacuum to an orange oil. Column chromatography on silica gel with 0-5% methanol/methylene chloride gave 0.22 g of the title compound. 1H-NMR (CDCl3): doublet 8.8 δ (1H); doublet 8.25 δ (1H); doublet 7.8 δ (2H); doublet 7.6 δ (1H); multiplet 7.3 δ (4H); multiplet 4.4 δ (1H); doublet 4.3 δ (2H); multiplet 2.9 δ (2H); singlet 2.4 δ (3H); multiplet 2.0 δ (2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06930109B2
Source datasetuspto-grants-2005_08
ORD IDord-cf7a8acb547f4c7397843dfc0b1549ff
Source noteuspto-grants-2005_08