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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793659Generated: November 4, 2026

Sodium Chloride → 2-Hydroxy-3-benzylsuccinate diethyl ester

https://huagongshe.com/reaction/1793659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantNADP nicotinamide-adenine-dinucleotide phosphateHCID 5886—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
ReactantDiethyl 2-benzyl-3-oxopentanedioateHCID 12200242—
Product2-Hydroxy-3-benzylsuccinate diethyl esterHCID 12567691—

Reaction Steps

The procedure of Example 4 was repeated for the screening of the KRED-8000 kit with 3-benzyloxaloacetate diethyl ester. Enzymes KRED 1008 and KRED 1004 showed complete reduction to the alcohol. Both reactions were repeated in larger scale for the purpose of isolating the product and verifying the structure using 1H NMR spectroscopy. In 20 mL of an aqueous solution containing 250 mM potassium phosphate (pH 6.7), 5% (v/v) polyethelene glycol (MW 1450) 0.5 M sodium chloride, 0.076 g of NADP+, 3.5 g of D-glucose 0.1 g of both lyophilized enzymes glucose dehydrogenase and KRED 1004 or KRED 1008 0.5 g of 3-benzyloxaloacetate diethyl ester were added. The reactions were incubated at 37 C in a shake oven for 20 h before they were extracted with ethyl acetate. The organic layers were evaporated to dryness, and the alcohols were further purified using silica gel chromatography, before they were analyzed by 1H NMR. Both enzymes gave 2-hydroxy-3-benzylsuccinate diethyl ester as the only product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07081535B2
Source datasetuspto-grants-2006_07
ORD IDord-78349326ce1745d5a8f9bd4e604b64fd
Source noteuspto-grants-2006_07