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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422115Generated: October 31, 2026

Acetic Anhydride → HCID 56622940, compound

https://huagongshe.com/reaction/1422115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 18707032HCID 18707032—
ProductHCID 56622940HCID 56622940—

Reaction Steps

The general synthetic pathway outlined in example 81, step 5, and example 83 have been applied to proper starting materials in the preparation of 3-(4-benzyloxyphenyl)-5-hydroxymethylpyrrolo[2,1,5-cd]indolizine-1,2-dicarboxylic acid, which was reacted with acetic acid anhydride by the general synthetic principles outlined in example 23, step 8, to afford 5-acetoxymethyl-3-(4-benzyloxyphenyl)pyrrolo[2,1,5-cd]indolizine-1,2-dicarboxylic acid anhydride as red crystals in 86%. 1H-NMR (DMSO-d6, 300 MHz) δ: 2.17 (s, 3H); 5.22 (s, 2H); 5.67 (s, 2H); 7.19 (d, 2H); 7.32-7.48 (m, 3H); 7.52 (d, 2H); 8.10-8.19 (m, 2H); 8.27 (d, 2H); 8.34 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080754
Source datasetuspto-grants-2000_06
ORD IDord-0aabe9bfa712466794b5bc2f0dab23d3
Source noteuspto-grants-2000_06