HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482207Generated: October 31, 2026
Ethylenediaminetetraacetic Acid → HCID 54350893, compound
https://huagongshe.com/reaction/482207
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylenediaminetetraacetic Acid | HCID 6049 | — |
| Reactant | Triethanolamine | HCID 7618 | — |
| Reactant | HCID 15677762 | HCID 15677762 | — |
| Product | HCID 54350893 | HCID 54350893 | 33% |
Reaction Steps
The acceptor aldehyde, 3-thioglyceraldehyde (Compound 3), was prepared by the method of Effenberger. [Effenberger Tetrahedron Lett., 33:5157 (1992)]. DERA (400U) was added to a 10 mL solution containing the acceptor aldehyde (100 mM Compound 3) and donor aldehyde (300 mM acetaldehyde), triethanolamine buffer (100 mM, pH 7.3) and EDTA (1 mM). This reaction is shown in Scheme 1. The resulting solution was stirred in the dark for 2 days under a N2 atmosphere. The reaction was quenched by addition of 2 volumes of acetone and cooling to 0° C. for 20 minutes. The precipitated protein was removed by centrifugation. After removal of the solvent under reduced pressure, a 33 percent yield of Compound 4 was obtained (characterized as 2-deoxy-5-thio-1,3,4-tri-O-acetyl-D-erythro-pentose). Compound 4 was purified from the residue by preparative TLC on silica (methanol/chloroform/hexane, 1:90:10).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05795749 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-fd907b13486c4e71af8262b14973c3b2 |
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| Source note | uspto-grants-1998_08 |
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