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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192741Generated: November 1, 2026

Acetic Anhydride → HCID 14522075, compound

https://huagongshe.com/reaction/1192741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant3-(2-Propyn-1-yloxy)benzenemethanolHCID 10797067—
CatalystSulfuric AcidHCID 1118—
SolventDichloromethaneHCID 6344—
ProductHCID 14522075HCID 14522075—

Reaction Conditions

Temperature0 °C

Reaction Steps

A 5.0 L flange flask was charged with 3 (706 g, approx. 4.36 mol, 1 eq) and acetic anhydride (99.5%, ex. Fisher, 1300 ml, 1 mol) to give a clear solution. Sulfuric acid (conc. 98%, 150 drops, ˜3 ml, catalytic) was then added very slowly (dropwise) over 30 minutes, with cooling to 0° C. by aid of an ice/water bath to control the exotherm to give a very dark reaction mixture. Maximum internal temperature observed was 45° C. After the addition the reaction mixture was stirred for 30 min, then the reaction mixture was stirred at 99° C. for 3 h. TLC-examination (silica-gel plate, DCM eluent, PMA stain) showed that all the starting material had been consumed. The mixture was cooled to room temperature (r.t.) overnight to give a dark green solution, which was poured onto an ice-water mixture (2.5 L water and 2.5 Kg of ice) with vigorous stirring. The product was extracted with DCM (5.0 L×3), and the combined extracts washed with water (3.0 L×3), dried over Na2SO4, and evaporated to give a black/brown oily residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680265B2
Source datasetuspto-grants-2014_03
ORD IDord-75312b6558af4077b975a0ec19419a87
Source noteuspto-grants-2014_03