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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894845Generated: October 26, 2026

DL-Phenylalanine, methyl ester → N-(Benzyloxycarbonyl)-L-aspartyl-L-phenylalanine methyl ester

https://huagongshe.com/reaction/894845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDL-Phenylalanine, methyl esterHCID 75737—
ReactantCalcium acetate monohydrateHCID 82163—
ReactantSodium AcetateHCID 517045—
ReactantL-Phenylalanine, methyl esterHCID 736234—
ReactantN-(Benzyloxycarbonyl)aspartic acidHCID 2723942—
SolventWaterHCID 962—
ProductN-(Benzyloxycarbonyl)-L-aspartyl-L-phenylalanine methyl esterHCID 1015963079.8%

Reaction Steps

The preparation of the immobilized enzyme and the reaction were conducted in the same manner as in Example 1 with the exception that: The quantity of Thermoase and that of the calcium acetate monohydrate were 9.0 g and 0.45 g respectively, the quantity of the 0.05 M sodium acetate buffer solution of pH 7.5 was 90 ml; the acrylic ester matrix carrier (Amberlite XAD-7, Trademark) was replaced with 16.6 g of another carrier of the similar class (Amberlite XAD-8, Trademark, containing about 150 wt.% of water on a dry basis; the quantity of N-benzyloxycarbonyl-L-aspartic acid was 2.14 g (8 m mol): L-phenylalanine methyl ester was replaced with 2.87 g (16 m mol) of DL-phenylalanine methyl ester; the quantity of the water saturated ethyl acetate solution was changed to 26 ml; and the reaction time was five fours. N-Benzyloxycarbonyl-L-aspartyl-L-phenylalanine methyl ester was obtained in the yield of 79.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284721
Source datasetuspto-grants-1981_08
ORD IDord-949b3636b8db411babdca52620009706
Source noteuspto-grants-1981_08