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HRID 2376856생성일: 2026년 10월 26일

Triethylamine → Tert-butyl 1,1-dioxo-1lambda6-thiomorpholine-4-carboxylate

https://huagongshe.com/reaction/2376856

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium ThiosulfateHCID 24477—
반응물m-Chloroperbenzoic acidHCID 70297—
반응물Thiomorpholine, N-BOC protectedHCID 21949316—
반응물tert-Butoxycarbonyl dicarbonateHCID 86600350—
용매DichloromethaneHCID 6344—
생성물Tert-butyl 1,1-dioxo-1lambda6-thiomorpholine-4-carboxylateHCID 2194926091.6%

반응 단계

tert-Butyl thiomorpholine-4-carboxylate (1.91 g, 9.42 mmol) was dissolved in dichloromethane (50 ml); m-chloroperbenzoic acid (5.0 g, 19 mmol) was gradually added while cooled with ice bath, stirred, and under nitrogen atmosphere; and the reaction mixture was stirred at room temperature for 12 hours. After addition of a saturated aqueous solution of sodium thiosulfate, the reaction mixture was kept stirred for a while; and this was subjected to extraction with ethyl acetate, washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. Triethylamine (8.1 ml, 58 mmol) were added to the obtained crystals; and the reaction mixture was stirred at room temperature. tert-Butoxycarbonyl dicarbonate (13.3 ml, 58 mmol) was added thereto; and the reaction mixture was stirred at room temperature for 10 hours. The reaction mixture was concentrated under reduced pressure; and the obtained crystals were suspended with a solvent mixture of diethyl ether:ethanol=10:1, filtered off, washed with diethyl ether and dried under aeration to yield the title compound as colorless crystals (2.03 g, 8.63 mmol, 91.6%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07468380B2
출처 데이터셋uspto-grants-2008_12
ORD IDord-ca9ed8b2450f46f89d37934466d5ddf2
출처 메모uspto-grants-2008_12