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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377263Generated: October 30, 2026

Triethylamine → HCID 87732437, compound

https://huagongshe.com/reaction/2377263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactantp,p'-Dimethoxybenzhydryl alcoholHCID 69768—
ReactantHCID 178480813HCID 178480813—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 87732437HCID 87732437—

Reaction Conditions

Temperature50 °C

Reaction Steps

To 4,4′-dimethoxybenzhydrol (5.62 g, 23.0 mmol) was carefully added thionyl chloride (20.1 mL, 276 mmol) and the mixture was heated to reflux for about 1 hour. The solution was cooled, evaporated to dryness and the residue was dissolved in tetrahydrofuran (50 mL). This solution was then added to a solution of Example 326 (5.3 g, 14.0 mmol) and triethylamine (5.9 mL, 42.0 mmol) in tetrahydrofuran (100 mL). The reaction mixture was heated to about 50° C. for about 2.5 hours, cooled, diluted with water and extracted with ethyl acetate. The combined organic extracts were dried (Na2SO4), filtered and concentrated under vacuum, and the residue was purified by flash chromatography on silica gel using dichloromethane/methanol (10:1) as eluent to provide the desired product. MS (ESI): m/z 605 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468371B2
Source datasetuspto-grants-2008_12
ORD IDord-f8132b92f19040cc90667a023b284bdf
Source noteuspto-grants-2008_12