HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441806Generated: October 26, 2026
Acetic Acid → 2-Oxo-2-isopropoxy-3,3,5-trimethyl-5-diisopropylphosphono-1,2-oxaphospholane
https://huagongshe.com/reaction/441806
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzene | HCID 241 | — |
| Reactant | Mesityl oxide | HCID 8858 | — |
| Reactant | Phosphorous acid, bis(1-methylethyl) ester | HCID 21884976 | — |
| Reactant | 1,2-Oxaphospholane | HCID 22633861 | — |
| Catalyst | Sodium | HCID 5360545 | — |
| Product | 2-Oxo-2-isopropoxy-3,3,5-trimethyl-5-diisopropylphosphono-1,2-oxaphospholane | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04042649 |
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| Source dataset | uspto-grants-1977_08 |
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| ORD ID | ord-7c8386c4458b4555b4383f8e647479c8 |
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| Source note | uspto-grants-1977_08 |
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