돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 426997생성일: 2026년 10월 24일

Acetyl chloride → 2-(2-Pyridyloxy)acetyl chloride

https://huagongshe.com/ko/reaction/426997

반응식

참여 물질

역할이름HCID투입량
반응물Acetyl chlorideHCID 6367—
반응물Phosphorus pentachlorideHCID 24819—
반응물2-(2-Pyridyloxy)acetic acid hydrochlorideHCID 66975989—
생성물2-(2-Pyridyloxy)acetyl chlorideHCID 20544437—

반응 단계

To a mixture of 2-(2-pyridyloxy)acetic acid hydrochloride (1.5 g) and acetyl chloride (8 ml) was added at -30° C. phosphorus pentachloride (3.3 g), and the mixture was stirred at room temperature for 18 hours. Precipitated crystals were collected by filtration and washed with a small amount of acetyl chloride and diethyl ether and dried to give 2-(2-pyridyloxy)acetyl chloride (1.3 g). A mixture of 7-(D-2-phenylglycinamido)-3-methyl-3-cephem-4-carboxylic acid (2.5 g) and trimethylsilylacetamide (0.0288 mole) in methylene chloride (70 ml) was stirred for 1.5 hours. The solution was cooled to 3° C. and the above obtained 2-(2-Pyridyloxy)acetyl chloride was added thereto. The resultant mixture was stirred under ice-cooling for 2 hours and concentrated. To the residue was added ice-water and the resultant powder was filtrated and washed with acetone containing water and acetone in turn to give powder (1.4 g). The filtrate and washings were collected together and extracted with ethyl acetate four times. The ethyl acetate extracts were washed with water, dried and concentrated to give powder (0.4 g). Thus obtained powders (1.4 g) and (0.4 g) were combined together and recrystallized from methanol to give crystals (0.9 g) of 7-{D-2-[2-(2-pyridyloxy)acetamido]-2-phenylacetamido}-3-methyl-3-cephem-4-carboxylic acid, mp 209° to 211° C. (dec).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04172198
출처 데이터셋uspto-grants-1979_10
ORD IDord-ee18a8c11a42427d9f3538a97b42e2b7
출처 메모uspto-grants-1979_10