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HRID 253714생성일: 2026년 10월 26일
Phosphoramidic dichloride, bis(2-chloroethyl)- → 2-{[2-(diethylamino)ethyl]thio}ethyl N,N-bis(2-chloroethyl)phosphorodiamidate
https://huagongshe.com/reaction/253714
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phosphoramidic dichloride, bis(2-chloroethyl)- | HCID 96271 | — |
| 반응물 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 반응물 | 2-[2-(Diethylamino)ethylthio]ethanol | HCID 5256545 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-{[2-(diethylamino)ethyl]thio}ethyl N,N-bis(2-chloroethyl)phosphorodiamidate | HCID 86631217 | — |
반응 단계
To a solution of 2-[2-(diethylamino)ethylthio]ethanol (420 mg, 2.4 mmol) in tetrahydrofuran, cooled to −78° C., was added with stirring lithium bis(trimethylsilyl)amide (1.0M in tert-butyl methyl ether, 2.62 mL, 2.62 mmol), followed by a solution of N,N-bis(2-chloroethyl)phosphoramidic dichloride (680 mg, 2.62 mmol) in tetrahydrofuran (10 mL). The orange reaction mixture was stirred at −78° C. for 90 minutes, then allowed to warm to −20° C. and ammonia gas bubbled through it for 10 minutes. The reaction mixture was stirred for an additional 10 minutes, then poured into a separatory funnel containing water (200 mL) and dichloromethane (200 mL). The organic and aqueous layers were separated, and the aqueous layer washed with dichloromethane (3×200 mL). The organic layer and washings were combined, dried over magnesium sulfate, filtered, and the filtrate concentrated under reduced pressure to give a yellow oil. The oil was purified by chromatography on a 25 g silica column, eluting with 90% chloroform/10% (5% ammonium hydroxide in methanol), to give 2-{[2-(diethylamino)ethyl]thio}ethyl N,N-bis(2-chloroethyl)phosphorodiamidate as a clear oil, 97% pure by HPLC. MS (ES): m/z=380 [C12H28Cl2N3O2PS+H+].
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07872134B2 |
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| 출처 데이터셋 | uspto-grants-2011_01 |
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| ORD ID | ord-81ee05034a8a4d14b0d370aadb32d2ed |
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| 출처 메모 | uspto-grants-2011_01 |
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