Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085988Generated: November 2, 2026

Ammonia → Phthalide

https://huagongshe.com/reaction/1085988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2-Methylbenzoic acidHCID 8373—
ProductPhthalideHCID 6885—
Product2-Methylbenzoic acidHCID 8373—

Reaction Steps

Next, the ammonia-treated crude o-toluic acid is subjected to fractionation so as to separate pure o-toluic acid from high boiling point components such as o-phthalimide, phthalide, etc. As to the fractionator, a packed column or a plate column having 10 ore more theoretical plates can be used. Preferably, a plate column or a packed column having 10 to 30 theoretical plates is used as the fractionator and operated at 100 to 300 Torr., preferably 150 to 250 Torr., and a reflux ratio of about 3 to 20. If the pressure is smaller than 100 Torr., an azeotrope of o-toluic acid and phthalide is produced, thus impairing the purity of o-toluic acid. A higher pressure elevates the bottom temperature of the fractionator, in which case o-toluic acid tends to decompose or polymerize. The fractionator should, therefore, be operated at the bottom temperature of lower than 250° C. Crude o-toluic acid treated with ammonia is fed to the fractionator at a point below the middle of the column and where at least two, preferably three, theoretical plates are allocated for the stripping section. For example, when a distillation column with 30 theoretical plates is used, it is preferable to allocate 3 to 7 theoretical plates in the stripping section.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011987
Source datasetuspto-grants-1991_04
ORD IDord-9e3473c00d644139b527632d45fb9c68
Source noteuspto-grants-1991_04