Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401620Generated: November 1, 2026

Acetic Anhydride → HCID 54275696, compound

https://huagongshe.com/reaction/2401620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant1,4-DioxaneHCID 31275—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 54072328HCID 54072328—
ProductHCID 54275696HCID 54275696—

Reaction Conditions

Temperature90 °C

Reaction Steps

The product of Example 22 (260 mg) is dissolved in dioxan (20 mL). Sodium borohydride (90 mg) is added followed by the dropwise addition of acetic anhydride (142 mg). The reaction mixture is stirred at 90° C. The reaction is shown to be complete by TLC after 4 hours. The solvent is removed in vacuo and the residue is partitioned between ethyl acetate (100 mL) and water (100 mL). The organic layer is dried over MgSO4, filtered and the solvent is removed in vacuo. The product is purified by flash column chromatography (silica, n-hexane/ethyl acetate 4:1). TLC (silica, n-hexane/ethyl acetate 2:1 Rf=0.65).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796307B2
Source datasetuspto-grants-2014_08
ORD IDord-8cd1a8bc7a9d41c68602cb4033570d4c
Source noteuspto-grants-2014_08