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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815102Generated: October 30, 2026

Acetic Anhydride → HCID 54275696, compound

https://huagongshe.com/reaction/1815102

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 numberUS06878721B1
Source datasetuspto-grants-2005_04
ORD IDord-aabf35bcbd4e4d88a62a33084361d7a6
Source noteuspto-grants-2005_04