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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426666Generated: October 30, 2026

Acetic Acid → HCID 53656302, compound

https://huagongshe.com/reaction/426666

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 -0° C. with 6.6 ml. of 3M 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, 14.35μ . NMR: δ3.93 (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 (theory 515), M+ -H2O at m/e 497.2776 (theory 497/2776.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04170710
Source datasetuspto-grants-1979_10
ORD IDord-0c46e1211e1d42aa8a3fb90c348df7d8
Source noteuspto-grants-1979_10