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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616434Generated: November 1, 2026

Acetic Anhydride → HCID 12764994, compound

https://huagongshe.com/reaction/1616434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantBoron trifluoride etherateHCID 8000—
Reactanttert-Butyl(dimethyl)[(prop-2-yn-1-yl)oxy]silaneHCID 3445622—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12764994HCID 12764994—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of tert-butyldimethyl(prop-2-yn-1-yloxy)silane (20.0 g, 116.9 mmol) in THF (400 mL) at −78° C. was added n-BuLi (90 mL, 140.0 mmol) and the reaction mixture was allowed to attain room temperature with in 2 h. Then the reaction mixture was cooled to −78° C. and borontrifluoride etherate (18 mL, 140.0 mmol) was added. After 10 minutes stirring acetic anhydride (15 mL, 153.0 mmol) was added and the reaction mixture was allowed to attain room temperature with in 2.5 h. Reaction was quenched with aqueous 1N NaOH solution and extracted with ethyl acetate (3 times). Combined organic layer was dried over sodium sulphate. Removal of the solvent under reduced pressure followed by solvent washings afforded C (13 g, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765732B2
Source datasetuspto-grants-2014_07
ORD IDord-8abb0d3d0ad242e79d29f578c1f2a153
Source noteuspto-grants-2014_07