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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1156502생성일: 2026년 10월 23일

Triethylamine → O,O-diethyl isopropyl[[(fluorocarbonyl)methylamino]thio]phosphoramidothioate

https://huagongshe.com/ko/reaction/1156502

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methyl N-hydroxyethanimidothioateHCID 92243—
반응물Phosphoramidothioic acid, (1-methylethyl)-, O,O-diethyl esterHCID 778771—
반응물N-chlorothio(methyl)carbamoyl fluorideHCID 12922862—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물O,O-diethyl isopropyl[[(fluorocarbonyl)methylamino]thio]phosphoramidothioateHCID 86737875—

반응 단계

A solution of O,O-diethyl isopropylphosphoramidothioate(14.9 g, 70.8 mmol) and triethylamine (9.8 ml, 70.8 mmol) in tetrahydrofuran (50 ml) is added dropwise over 10 minutes to a solution of N-chlorothio(methyl)carbamoyl fluoride (10.2 g, 70.8 mmol) in tetrahydrofuran (50 ml) cooled in an ice bath. After the addition the mixture is stirred for 1.5 hours at 0°, diluted with ether (200 ml), washed with ice cold water, dried over sodium sulfate and concentrated under reduced pressure. The residue shows identical absorptions in the ir and pmr spectra for νC=O and N--CH3 as obtained for the yellow oil that is intermediate II1 of Example 1. The crude II1 product is suitable for reaction with methyl N-hydroxyethanimidothioate as in Example 1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04336207
출처 데이터셋uspto-grants-1982_06
ORD IDord-3fc776fce7f74d8bb864eb11f6607529
출처 메모uspto-grants-1982_06