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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1445367생성일: 2026년 10월 24일

Isopropyl Acetate → (R)-N-Methoxy-3-(4-methoxybenzyl)-N-methyl-2-oxothiazolidine-4-carboxamide

https://huagongshe.com/ko/reaction/1445367

반응식

참여 물질

역할이름HCID투입량
반응물Isopropyl AcetateHCID 7915—
반응물4-MethylmorpholineHCID 7972—
반응물N,O-DimethylhydroxylamineHCID 14232—
반응물Pivaloyl chlorideHCID 62493—
반응물(R)-3-(4-Methoxybenzyl)-2-oxothiazolidine-4-carboxylic AcidHCID 11207876—
용매HeptaneHCID 8900—
생성물(R)-N-Methoxy-3-(4-methoxybenzyl)-N-methyl-2-oxothiazolidine-4-carboxamideHCID 1674259270%

반응 조건

온도0 °C

반응 단계

A 22 L three-necked round bottom flask fitted with an internal temperature probe and a mechanical stirrer was charged with the title compound from Example 3 (310.0 g, 1.16 mol) and isopropyl acetate (2.4 L). The vessel was purged with nitrogen and cooled to 0° C. N-methylmorpholine (130.0 g, 1.29 mol) was added dropwise such that the internal reaction temperature never increased above 5° C. The reaction became cloudy. Pivaloyl chloride (150.0 g, 1.24 mol) was added dropwise such that the internal reaction temperature never increased above 5° C. The reaction was stirred at 0° C. for 45 minutes. N-methoxy-methanamine (78.0 g, 1.28 mol) was added dropwise, again keeping the internal reaction temperature below 5° C. The reaction was monitored by HPLC and was worked up when the ratio of the product to starting material was 4:1 (approximately 30 minutes after amine addition). The mixture was then washed with 0.1 M HCl and satd aq NaHCO3. The organic phase was separated and concentrated to a final volume of 1.0 L by distillation. Upon stirring, a precipitate began to form. A 250 mL portion of n-heptane was added, and the mixture was stirred vigorously. The solid was filtered and dried in a vacuum oven at 40° C. to afford the title compound (250 g, 70%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07666861B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-f079e57d90744fd5929e0781bd3a0bf9
출처 메모uspto-grants-2010_02