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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258626Generated: October 31, 2026

Acetic Acid → HCID 53656302, compound

https://huagongshe.com/reaction/258626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 70607475HCID 70607475—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53656302HCID 53656302—

Reaction Steps

A solution of 1.88 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 6.6 ml. of 3 M phenyl 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 with magnesium sulfate, the extract was evaporated and the residue chromatographed on silica. Elution with 30% ethyl acetate in hexane gave 0.90 g. of the title product as an oil, λmaxfilm 3.00 (shoulder), 3.50, 5.88, 6.28, 6.47, 6.95, 7.25, 13.30, 14.35 μ. NMR: δ 3.93 (S, 4, ketal), 4.35 (M, 2, --CH2NO2), 5.15-6.05 (M, 4, olefinic --H), 5.88 (S, 2, -OH), 7.45 (M, 5, aromatic-HO ppm. Mass spectrum: M+ at m/e 515 (theory 515), M+--H2O at m/e 497.2776 (theory 497.2776.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04034002
Source datasetuspto-grants-1977_07
ORD IDord-1c534bc540d943c2a0d130df532bac92
Source noteuspto-grants-1977_07