Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165239Generated: October 30, 2026

Chloroacetic Acid → O-(2-diazo-3-hydroxy-1-oxopropyl)-L-serine

https://huagongshe.com/reaction/2165239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetic AcidHCID 300—
ReactantO-(L-serinyl)-N-trifluoroacetyl-L-serineHCID 18640004—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductO-(2-diazo-3-hydroxy-1-oxopropyl)-L-serineHCID 5432497811.7%

Reaction Steps

To a solution of O-(L-serinyl)-N-trifluoroacetyl-L-serine (400 mg) and 4M aqueous chloroacetic acid (50 μl) is water (4 ml) was added sodium nitrite (193 mg) at room temperature. After stirring for 15 minutes at room temperature, the reaction mixture was neutrized with 2M tris buffer solution to pH 7.0 to 7.3 and then Acylase I (acylase, Sigma A-7264, made by Sigma Chemicals) (60 mg) was added. The mixture was stirred for 5 hours at room temperature, and chromatographed on carbon (50 ml) eluting successively with water and a 9:1 mixture of water and acetone to give a crude product, which was chromatographed on silica gel eluting with a mixture of methylene chloride, methanol and water (10:6:1 to 5:3:1), and also chromatographed on silica gel eluting with a 5:3:1 mixture of methylene chloride, methanol and water (5:3:1) to give a pure product which was lyophylized to give O-(2-diazo-3-hydroxy-1-oxopropyl)-L-serine (33 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939241
Source datasetuspto-grants-1990_07
ORD IDord-f5adcc03ebf34845b7d226ea310b3626
Source noteuspto-grants-1990_07