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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605502Generated: November 2, 2026

Acetic Anhydride → HCID 23277624, compound

https://huagongshe.com/reaction/1605502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 23277598HCID 23277598—
SolventAcetic AcidHCID 176—
ProductHCID 23277624HCID 23277624—

Reaction Steps

To a suspension of 1.21 g. (2 mmole) of 5-amino-3-methyl-6-{7-ethyl-4-hydroxy-3,5-dimethyl-6-oxo-7-[5-ethyl-3-methyl-5-(5-ethyl-5-hydroxy-6-methyl-2-tetrahydropyranyl)-2-tetrahydrofuryl]-heptyl}salicylic acid in 50 ml. glacial acetic acid was added 1 ml. acetic anhydride (~10 mmoles). On warming the mixture to 70° on a steam bath, the amine dissolved and after a further half an hour at room temperature, the solution was poured on to crushed ice. The mixture was carefully made alkaline with sodium carbonate solution and extracted twice with 400 ml. ether. After drying (NaSO4) the ethereal solution was evaporated to approximately 100 ml. The resulting microcrystalline product had m.p. 189°-190°, [α]D -17.45° (1%, MeOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03950320
Source datasetuspto-grants-1976_04
ORD IDord-9917288a3b534dd18d6d6efe519f4e6e
Source noteuspto-grants-1976_04