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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16925생성일: 2026년 10월 25일

Pentane → Di-tert-butyl-trimethylsilylmethyl-phosphane

https://huagongshe.com/reaction/16925

반응식

참여 물질

역할이름HCID투입량
반응물PentaneHCID 8003—
반응물Ammonium ChlorideHCID 25517—
반응물Di-tert-butylchlorophosphineHCID 139566—
반응물HCID 178418939HCID 178418939—
용매TetrahydrofuranHCID 8028—
생성물Di-tert-butyl-trimethylsilylmethyl-phosphaneHCID 12583313—

반응 단계

50.00 g (0.277 mol) of Di-t-butylchlorophosphine, 304 ml of 1.0 M pentane solution of (trimethylsilylmethyl)lithium and 150 ml of THF) were refluxed under argon for 3 days. The reaction mixture was allowed to cool off to RT and an aqueous solution of ammonium chloride was added slowly. The organic phase was separated, and dried with magnesium sulfate. After removal of the solvent, the product was purified by distillation in vacuum. The yield of di-tert-butyl-trimethylsilanylmethyl-phosphane was 55.32 g (86%) with b.p. 50-52° C./0.5 mm. 31P NMR (C6D6)+20.05 ppm. 1H NMR (C6D6) 0.01 (s, 9H, SiMe3), 0.23 (d, 2H, 2JPH=5.34 Hz, P—CH2—SiMe3), 0.91 (s, 9H, Me3C), 0.93 (s, 9H, Me3C). Anal. Calcd. for C12H29PSi: C, 62.01; H, 12.58; P, 13.33. Found: C, 61.89; H, 12.53; P, 13.25.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737277B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f020141d60174cacaa5888e5bc63f7cc
출처 메모uspto-grants-2010_06