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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252421Generated: October 30, 2026

Acetic Anhydride → HCID 57308684, compound

https://huagongshe.com/reaction/1252421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 15051730HCID 15051730—
SolventPyridineHCID 1049—
ProductHCID 57308684HCID 57308684—

Reaction Steps

6,9-Dihydroxy-8-hydroxymethyl-14-oxa-1,11-diazatetracyclo[7.4.1.02,7.010,12 ]tetradeca-2,4,6-triene-4-carbaldehyde (4 mg) was dissolved in pyridine (1 ml). To this solution was added acetic anhydride (50 μl) and the mixture was allowed to stand at room temperature overnight. The reaction mixture was evaporated to dryness in vacuo and the residual oil was subjected to preparative thin layer chromatography, which was developed with a mixture of methanol and chloroform (5:95, v/v) to yield 8-acetoxymethyl-11-acetyl-4-formyl-9-hydroxy-14-oxa-1,11-diazatetracyclo[7.4.1.02,7.010,12 ]tetradeca-2,4,6-trien-6-yl acetate (1.5 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04743555
Source datasetuspto-grants-1988_05
ORD IDord-fe5a3a86935845b59518c87b9d493965
Source noteuspto-grants-1988_05