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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658191Generated: October 30, 2026

Triethylamine → Phthalide

https://huagongshe.com/reaction/1658191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1(3H)-Isobenzofuranone, 3-bromo-HCID 96218—
SolventAcetoneHCID 180—
ProductPhthalideHCID 6885—

Reaction Steps

A solution of 6-tritylaminopenicillanic acid (9.8 g; 0.02M) in dry acetone (100 ml.) was cooled to 0°C, triethylamine (2.9 mg. 0.02 M) was added, followed by 3-bromophthalide (4.1 g; 0.02M) in dry acetone (20 ml.), and the reaction mixture kept at 0°C with stirring for 2 hours and finally at ambient temperatures for 1 hour. The triethylammonium bromide which precipitated was removed by filtration, the evaporated filtrate was dissolved in ethyl acetate (150 ml.) and after two washings with cold 2% aqueous sodium bicarbonate (2 × 150 ml.) and with ice-water (2 × 100 ml.) the ethyl acetate layer was dried over anhydrous magnesium sulphate to yield, on removal of solvent in vacuo, phthalide 6-tritylaminopenicillanate as a white amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03963702
Source datasetuspto-grants-1976_06
ORD IDord-663d086fb34142a685f21f733463b869
Source noteuspto-grants-1976_06