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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111504Generated: October 30, 2026

Atrolactic acid → (S)-Atrolactic acid

https://huagongshe.com/reaction/2111504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAtrolactic acidHCID 1303—
ReactantN-PhenylglycineHCID 66025—
Reactant2-Chloromandelic acidHCID 97720—
Product(S)-Atrolactic acidHCID 445144—

Reaction Steps

The analysis of phenyllactic acid was initially plagued with the same problems discussed for phenylglycine and 2-chloromandelic acid. However, in this case, adjustment of the solvent concentration in the nonchiral HPLC method led to a shift in the retention time of the acid, so that it no longer coeluted with the cell lysate peak. Following this, no problems were encountered with either the nonchiral or chiral methods. Representative nonchiral chromatograms of the product (1.9 min) and cyanohydrin substrate (3.7 min) are shown in FIG. 8A, while the chiral analysis of the acid is shown in FIG. 8B, with the L-enantiomer eluting at 2 min and the opposite enantiomer at 6 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521216B2
Source datasetuspto-grants-2009_04
ORD IDord-e7a7773fc4774166a726df16c81889c8
Source noteuspto-grants-2009_04