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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495334Generated: October 26, 2026

Phenylalanine ethyl ester → L-Phenylalanine

https://huagongshe.com/reaction/495334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylalanine ethyl esterHCID 76506—
ReactantLactic acid phenylalanineHCID 69440103—
SolventIsopropanolHCID 3776—
ProductL-PhenylalanineHCID 614080%

Reaction Steps

The lactic acid was esterified with iso-propyl alcohol and was used along with the phenylalanine ethyl ester. An oligomerization yield of 80% was obtained with respect to phenylalanine. The positive and negative ion spectrum is provided in FIGS. 59A and 59B respectively. The positive ion spectrum reveals the strong presence of sodiated co-oligomers ions of NLA-(Phe)3-PheC-OEt+Na+ and NLA-(Phe)4-PheC-OEt+Na+ at masses 730 and 877 respectively. These peaks are separated by 147 units, which is the repeating residue unit of phenylalanine. The absence of any oligomer peaks is due to fact that the phenylaline does not oligomerize without a N-terminal starter molecule. This points to the presence of LA at the N-terminal end of the oligomer. The presence of ethyl ester (and absence of the iso-propyl ester) at the C-terminal end also reinforces this result. The negative ion spectrum reveals two sets of peaks with each set separated by 147 units. These sets represent the deprotonated co-oligomer peaks to form NLA-Phen-PheC-OEt with n having values of 3 and 4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939693B2
Source datasetuspto-grants-2005_09
ORD IDord-ac02a61fa991462a9cb95cc39340ae9a
Source noteuspto-grants-2005_09