Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetone → 1,3-Propanediol, 2-(4-pentenyl)-
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetone | HCID 180 | — |
| 반응물 | Diethyl 2-pent-4-enylpropanedioate | HCID 361718 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1,3-Propanediol, 2-(4-pentenyl)- | HCID 11094751 | 84.9% |
반응 단계
A suspension of 13.8 g of lithium aluminium hydride in 500 ml of tetrahydrofuran was treated dropwise under nitrogen at 0°-5° C. within 1 hour with a solution of 33.2 g of diethyl (4-pentenyl)malonate in 125 ml of tetrahydrofuran. The mixture was stirred overnight at room temperature and then heated to boiling for 3 hours. After cooling there were cautiously added dropwise to the reaction mixture firstly 25 ml of acetone and then 25 ml of saturated sodium hydrogen carbonate solution. The resulting slurry was suction filtered and the residue on the suction filter was washed four times with tetrahydrofuran. Concentration of the filtrate gave 17.8 g of 2-(4-pentenyl)-1,3-propanediol (purity 89%) as a yellow liquid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04709030 |
| 출처 데이터셋 | uspto-grants-1987_11 |
| ORD ID | ord-2cfe4bbc3277479d8c5031fa66304d2a |
| 출처 메모 | uspto-grants-1987_11 |