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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7655생성일: 2026년 10월 23일

Dichloromethane → 4-(2,2-Dimethylpropionyloxy)pyrazolidine-1,2-dicarboxylic acid 1-benzyl ester 2-tert-butyl ester

https://huagongshe.com/ko/reaction/7655

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Pivaloyl chlorideHCID 62493—
반응물1-Benzyl 2-(tert-butyl) 4-hydroxypyrazolidine-1,2-dicarboxylateHCID 20724753—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매PyridineHCID 1049—
생성물4-(2,2-Dimethylpropionyloxy)pyrazolidine-1,2-dicarboxylic acid 1-benzyl ester 2-tert-butyl esterHCID 2072475198%

반응 단계

4-Hydroxypyrazolidine-1,2-dicarboxylic acid 1-benzyl ester 2-tert-butyl ester, 28, (1.42 mg, 4.40 mmol) is dissolved in pyridine (22 mL). 4-Dimethylamino-pyridine (10 mg) is added followed by trimethylacetyl chloride (1.63 mL, 13.2 mmol). The reaction is stirred at ambient temperature for 12 hours. The cloudy reaction mixture is then concentrated in vacuo to afford a white residue. Dichloro-methane (75 mL) is added to the residue and the mixture washed with a 1.0 N aqueous solution of hydrochloric acid (75 mL). The aqueous layer is extracted with dichloro-methane (75 mL), the combined organic layers washed with a saturated aqueous solution of NaHCO3 (75 mL), water (75 mL), brine (75 mL), then dried, filtered and concentrated in vacuo to afford the crude product. The crude product is purified over silica (4:1 to 1:1 hexane/ethyl acetate) to afford 1.76 g (98% yield) of the desired product as a clear, viscous oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087615B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-bd9ac4cd0e8844958d4762bd71e90a7b
출처 메모uspto-grants-2006_08