참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | Potassium Phosphate, Tribasic | HCID 62657 | — |
| 반응물 | Lithium phosphate | HCID 165867 | — |
| 반응물 | 4-Oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3-(2-hydroxyethylidene)-7-oxo-, lithium salt (1:1), (2R,3Z,5R)- | HCID 23714647 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | Potassium Clavulanate | HCID 23665591 | 81% |
반응 단계
Lithium clavulanate (5.15 g, estimated purity 95% pfa; 0.025 moles) was dissolved in water (45 mls) and cooled in an ice bath. Tripotassium orthophosphate (10.1 mls of 1 M solution; 1.2 equivalents) was added in one lot. Ethanol (32 mls) was added slowly over 1/2 hour by which time lithium phosphate had precipitated out and the pH had fallen from 8.3 to 7.3. The mixture was then made up to 800 mls with acetone over 3/4 hr. Celite (2 gm) was added and then the mixture was filtered to give a clear, colourless filtrate. This was added with rapid stirring to acetone (1750 mls) over 1 hr and the white solid was filtered off, washed with acetone (3×50 mls) and dried on a fluid bed dryer to yield potassium clavulanate (4.8 g, 82.9 pfa, 81% recovery).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04255332 |
|---|
| 출처 데이터셋 | uspto-grants-1981_03 |
|---|
| ORD ID | ord-93c4962afafc47268f71341e3f652412 |
|---|
| 출처 메모 | uspto-grants-1981_03 |
|---|
