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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 481081생성일: 2026년 10월 26일

Sodium Iodide → 5-acetyl-4-oxo-5,6,7,8-tetrahydro-4H-cyclohepta[b]pyrrole-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester

https://huagongshe.com/reaction/481081

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Acetyl chlorideHCID 6367—
반응물Bismuth trichlorideHCID 24591—
반응물4-trimethylsilanyloxy-7,8-dihydro-6H-cyclohepta[b]pyrrole-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl esterHCID 20762225—
용매Ethyl ether methylene chlorideHCID 21881112—
생성물5-acetyl-4-oxo-5,6,7,8-tetrahydro-4H-cyclohepta[b]pyrrole-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl esterHCID 2060565486%

반응 단계

Bismuth (III) chloride (0.1 mmol) and sodium iodide (0.3 mmol) are transferred to a dried flask under nitrogen and 5 mL of a mixture of CH2Cl2/ether (9/1) is added by a syringe. This is followed by the addition of acetyl chloride (2.2 mmol) and the suspension is stirred for 5 min at RT. 4-trimethylsilanyloxy-7,8-dihydro-6H-cyclohepta[b]pyrrole-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester (2 mmol) in 5 mL of the same solvent mixture is added. After 2 hours at RT, the mixture is quenched with 20 mL saturated NaHCO3 solution and extracted several times with CH2Cl2. The organic layers are combined, dried over Na2SO4 and evaporated in vacuo yielding 5-acetyl-4-oxo-5,6,7,8-tetrahydro-4H-cyclohepta[b]pyrrole-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester as an oil (86%). LRMS 363.4 found (M+1) 364.2

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06653471B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-d3e8e5426a5845489a4b72e08857e8b7
출처 메모uspto-grants-2003_11