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HRID 1013491作成日:2026年10月27日

Triethylamine → tert-Butyl 3-methyl-2,4-dioxa-9-aza-3-phosphaspiro[5.5]undecane-9-carboxylate 3-oxide

https://huagongshe.com/reaction/1013491

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methyl phosphonic dichlorideHCID 12671—
反応物Tert-butyl 4,4-bis(hydroxymethyl)piperidine-1-carboxylateHCID 21955203—
溶媒DichloromethaneHCID 6344—
溶媒Sodium BicarbonateHCID 516892—
生成物tert-Butyl 3-methyl-2,4-dioxa-9-aza-3-phosphaspiro[5.5]undecane-9-carboxylate 3-oxideHCID 57925809—

反応条件

温度0 °C

反応手順

Et3N (943 μL, 6.76 mmol) and tert-butyl 4,4-bis(hydroxymethyl)piperidine-1-carboxylate (790 mg, 3.22 mmol) were combined in CH2Cl2 (25 mL) and cooled to 0° C. A solution of methylphosphonic dichloride (428 mg, 3.22 mmol) in CH2Cl2 (20 mL) was added dropwise over 1 h. The reaction was then allowed to warm to room temperature over 1 h. It was subsequently diluted with saturated NaHCO3 and extracted with CH2Cl2 (2×). The combined organic layers were washed with brine, dried (MgSO4), and evaporated to give the desired product as a colorless solid that was used without purification. MS: cal'd 306 (MH+), exp 306 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07981874B2
出典データセットuspto-grants-2011_07
ORD IDord-2dd70295602744fcb0fe139c4ce2d304
出典メモuspto-grants-2011_07