HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Pyroglutamic Acid → tetrabutylphosphonium (S)-(-)-2-pyrrolidone-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Pyroglutamic Acid | HCID 7405 | — |
| Reactant | Phosphonium, tetrabutyl-, hydroxide (1:1) | HCID 84487 | — |
| Product | tetrabutylphosphonium (S)-(-)-2-pyrrolidone-5-carboxylate | HCID 86626712 | 105.5% |
Reaction Steps
At 0° C., 4.2 g of (S)-(−)-2-pyrrolidone-5-carboxylic acid (by Wako Pure Chemical Industry) was added to 21.3 g of tetrabutylphosphonium hydroxide (aqueous 41.4% solution, by Hokko Chemical), and stirred for 10 minutes. Using an evaporator, the pressure was reduced to 40 to 50 mmHg, and this was concentrated at 60 to 80° C. for 2 hours, and then at 90° C. for 3 hours. Thus, 13.3 g of tetrabutylphosphonium (S)-(−)-2-pyrrolidone-5-carboxylate (purity: 94.1%) was obtained as an oily compound. The obtained ionic liquid had the same properties as in Production Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09018321B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-ca6fa63665f8497bb6791eb286a5f0c7 |
| Source note | uspto-grants-2015_04 |