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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471394Generated: October 30, 2026

Acetic Anhydride → HCID 131732748, compound

https://huagongshe.com/reaction/1471394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium AcetateHCID 517045—
ReactantHCID 131732747HCID 131732747—
SolventSodium HydroxideHCID 14798—
ProductHCID 131732748HCID 13173274892%

Reaction Conditions

Temperature80 °C

Reaction Steps

A part of the crude trans-methyl 9-hydroxy-7-methylspiro[4.5]dec-7-ene-6-carboxylate obtained (4.0 g) was treated with acetic anhydride (3.5 ml, 37.4 mmol) and sodium acetate (1.46 g, 17.8 mmol). The resulting mixture was stirred at 80° C. for 4 h, poured into cold 2N aqueous NaOH (20 ml), and extracted twice with MTBE (30 ml). The combined organic phases were washed with water (30 ml), with a saturated aqueous solution of NaCl (30 ml), dried (MgSO4), concentrated giving crude trans-methyl 9-acetoxy-7-methylspiro[4.5]dec-7-ene-6-carboxylate (4.4 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012391B2
Source datasetuspto-grants-2015_04
ORD IDord-06d3009681454879998f427b464f9e63
Source noteuspto-grants-2015_04