Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → [4-Cyano-2,3-bis-[(2-methoxy-ethoxy)-methoxy]-phenyl]bromoacetic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Bromoform | HCID 5558 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 1,4-Dioxane | HCID 31275 | — |
| 반응물 | Lithium Bromide | HCID 82050 | — |
| 반응물 | 4-Cyano-2,3-bis-[(2-methoxy-ethoxy)-methoxy]-benzaldehyde | HCID 18359078 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | [4-Cyano-2,3-bis-[(2-methoxy-ethoxy)-methoxy]-phenyl]bromoacetic acid | HCID 18359186 | — |
반응 단계
440 microliters of bromoform were added at -5° C. to a mixture of 4.26 mg of lithium bromide, 598 mg of potassium hydroxide and 5 ml of water and then, a solution of 825 mg of a 4-cyano-2,3-bis-[(2-methoxy-ethoxy)-methoxy]-benzaldehyde (preparation given hereafter) in 5 ml of dioxane was added dropwise. The mixture was stirred for 72 hours at 0° C. to -5° C. and was poured into a stirred mixture at 0° C. to -5° C. of 15 ml of ethyl acetate and 11 ml of hydrochloric acid. Extraction was carried out with ethyl acetate and the extracts were washed, dried and evaporated to dryness under reduced pressure. The oil obtained was used as is for the following step.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05728828 |
| 출처 데이터셋 | uspto-grants-1998_03 |
| ORD ID | ord-a2d6a5f5e06e41cb9bec46be781f750a |
| 출처 메모 | uspto-grants-1998_03 |