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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622069Generated: November 1, 2026

Atrolactic acid → (S)-Atrolactic acid

https://huagongshe.com/reaction/1622069

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 numberUS08778651B2
Source datasetuspto-grants-2014_07
ORD IDord-5bc63c2806c04ce085a02098b28dc4d7
Source noteuspto-grants-2014_07