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HRID 408976作成日:2026年10月25日

Dichloromethane → (2S)-neopentyl 2-(chloro-(naphthalene-1-yl)phosphorylamino)-propanoate

https://huagongshe.com/reaction/408976

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物TriethylamineHCID 8471—
反応物1-DichlorophosphoryloxynaphthaleneHCID 575631—
反応物(S)-neopentyl 2-aminopropanoate p-toluenesulfonic acidHCID 86662564—
生成物(2S)-neopentyl 2-(chloro-(naphthalene-1-yl)phosphorylamino)-propanoateHCID 86662566—

反応手順

Naphthalene-1-yl phosphorodichloridate (1219 g, 4.67 mol) and (S)-neopentyl 2-aminopropanoate p-toluenesulfonic acid (1547 g, 4.67 mol) were suspended in anhydrous dichloromethane (15 L) in a 22 L 3-neck flask equipped with a mechanical stirrer, an internal thermocouple, a cooling bath of dry/acetone, an additional funnel and a nitrogen inlet. Anhydrous triethylamine (1.3 L, 9.34 mmol, ≧99.5% grade, Product No 471283, Aldrich) was slowly added at −25° C. for one h. Later the reaction mixture was warmed to room temperature and stirred for overnight and monitored by 31P NMR. After completion, the solvent was removed under reduced pressure and the resulting crude residue that was triturated with a 1:1 mixture of ethyl acetate (2 L)/hexanes (2 L) was filtered by short pad of silica gel (Silicycle, SiliaFlash® P60, 3 inch high, funnel: 3 L medium size) and eluted using a mixture of ethyl acetate/hexanes (3 L: 3 L) followed by rinse with a mixture of ethyl acetate/hexanes (1.5 L: 1.5 L). Upon concentration, the dark oil was diluted with 3 L THF and was concentrated again under reduced pressure to deliver 1700 g (94%) of product which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08759318B2
出典データセットuspto-grants-2014_06
ORD IDord-348316c6b0694afcb76dd1eb0ad3afc5
出典メモuspto-grants-2014_06