Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482640Generated: October 30, 2026

Sulfuric Acid → HCID 178424156, compound

https://huagongshe.com/reaction/482640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactantethoxy(phenyl)phosphiniteHCID 18981701—
ReactantHCID 178418370HCID 178418370—
SolventDiethyl EtherHCID 3283—
ProductHCID 178424156HCID 17842415680.9%

Reaction Steps

A solution of p-tolylmagnesium bromide [prepared from p-bromotoluene (29.1 g, 0.16 mol) and magnesium (4.38 g, 0.18 g-atom)] in ether (100 mL) was treated with a solution of ethyl phenylphosphonite (13,6 g, 0.08 mol) in ether (50 mL) with vigorous mechanical stirring. The mixture was heated at reflux for 1/2 hr., then 100 mL of 25% sulfuric acid was added cautiously. Three layers formed; the bottom (aqueous) layer was extracted with toluene. Addition of NaHCO3 to the combined upper layers produced a vigorous reaction and a single organic phase. The organic phase was washed with water and with saturated NaCl, dried and evaporated to give an oil (14 g). Kugelrohr distillation at 120°-160° C. (0.1 mmHg) followed by chromatography on silica gel (CHCl3), then 10% MeOH--CHCl3) gave 7.1 g of an oil. This was distilled in the Kugelrohr again (150° C., 0.1 mmHg) to give 6.2 g of product which appears to be pure by NMR and crystallized on standing. 1H NMR (CDCl3) δ8.0-7.2 (m, 9H), 8.08 (d, J=480 Hz, 1H), 2.42 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04574060
Source datasetuspto-grants-1986_03
ORD IDord-2e2554719308478d8e2ff36647df4ef4
Source noteuspto-grants-1986_03