HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028256Generated: October 31, 2026
1-Butanol → 3-(Ethylhydroxyphosphinyl)-2-methylpropionic acid
https://huagongshe.com/reaction/1028256
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Butyl ethyl(2-cyano-2-methylethyl)phosphinate | HCID 86657307 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(Ethylhydroxyphosphinyl)-2-methylpropionic acid | HCID 46216500 | 96% |
Reaction Steps
A stirred apparatus is initially charged with 150 g of butanol, 65 g of water, 150 g (3.75 mol) of sodium hydroxide and 271 g (1.25 mol) of butyl ethyl(2-cyano-2-methylethyl)phosphinate (produced as in Example 9). The efficiently stirred mixture was heated to about 120° C. and reacted at that temperature for about 8 hours. Then, 250 ml of water were added and the butanol was removed from the reaction mixture by distillation. Following the addition of a further 500 ml of water, the mixture was neutralized by addition of about 184 g (1.88 mol) of concentrated sulfuric acid. The water is then distilled off in vacuo. The residue is taken up in tetrahydrofuran and extracted. The insoluble salts are filtered off. The solvent of the filtrate is removed in vacuo and the residue is recrystallized from acetone to obtain 216 g (96% of theory) of 3-(ethylhydroxyphosphinyl)-2-methylpropionic acid as a solid material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08735477B2 |
|---|
| Source dataset | uspto-grants-2014_05 |
|---|
| ORD ID | ord-fb97843e7a80471d932647c9b254262b |
|---|
| Source note | uspto-grants-2014_05 |
|---|