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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263142Generated: October 27, 2026

Acetic Acid → HCID 54508268, compound

https://huagongshe.com/reaction/263142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 70607475HCID 70607475—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54508268HCID 54508268—

Reaction Steps

A solution of 1.72 g. of 7-[8-nitromethyl-7-(3-oxo-1-octenyl)-1,4-dioxaspiro[4.4]non-6-yl]-5-heptenoic acid in 80 ml. of tetrahydrofuran was treated at -10° C. with 9.7 ml. of 3 M methyl magnesium bromide in tetrahydrofuran and was stirred at 0° C. for one hour. The reaction mixture was added to aqueous ammonium chloride solution, acidified with acetic acid and extracted with ether. After washing with water and drying over magnesium sulfate, the extract was evaporated and the residue chromatographed on silica. Elution with 30% ethyl acetate in hexane gave 0.26 g. of the title product as an oil, λmaxfilm 3.00 (shoulder), 3.45, 5.80 (shoulder), 5.85, 6.45, 7.25, 10.30μ. NMR: δ 1.32 (S, 15-methyl), 4.01 (S, 4, ketal), 4.4 (M, 2, CH2NO2), 5.22 (M, 2, 5 and 6-H), 5.63 (M, 2, 13 and 14-H) ppm. Mass spectrum: M+ at m/e 453), (theory 453), M+ --H2O at m/e 435.2571 (theory 435.2620).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04156094
Source datasetuspto-grants-1979_05
ORD IDord-21c98384cad94dfeae5cf1a8fd37a1a1
Source noteuspto-grants-1979_05