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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763803Generated: November 1, 2026

Acetic Acid → 2-Oxo-2-isopropoxy-3,3,5-trimethyl-5-diisopropylphosphono-1,2-oxaphospholane

https://huagongshe.com/reaction/1763803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzeneHCID 241—
ReactantMesityl oxideHCID 8858—
ReactantPhosphorous acid, bis(1-methylethyl) esterHCID 21884976—
Reactant1,2-OxaphospholaneHCID 22633861—
CatalystSodiumHCID 5360545—
Product2-Oxo-2-isopropoxy-3,3,5-trimethyl-5-diisopropylphosphono-1,2-oxaphospholaneHCID 54008312—

Reaction Steps

As described in Example 4, a mixture of 19.6 g of mesityl oxide (0.20 mole), 99.6 g of diisopropyl phosphite (0.60 mole) and 100 ml of benzene was reacted with 2.1 g of sodium as catalyst over the course of 10 minutes. The reaction was vigorously exothermic. After a subsequent reaction for 15 minutes at the boiling temperature, the reaction mixture was neutralized with 5.5 g of glacial acetic acid and diluted with 150 ml of benzene. After the reaction solution cooled, it was extracted with 20 ml of benzene twice, and the extract was combined with the chief portion, dried over Na2SO4 and concentrated in a rotary evaporator. The distillation yielded 27.5 g of a first fraction with a boiling point of 68°-75° C./10 mm Hg and consisting of virtually pure diisopropyl phosphite as well as 58.0 g (78.3%) of the oxaphospholane which boiled at 120°/0.02 mm Hg to 125° C./0.05 mm Hg; 5.3 g remained as residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04113669
Source datasetuspto-grants-1978_09
ORD IDord-bfa3e274de6d41fb8bcfb787a2084d6a
Source noteuspto-grants-1978_09