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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1677607생성일: 2026년 10월 24일

Benzyl chloroformate → 1-Carbobenzyloxyamino-2-methylpropanephosphonous acid

https://huagongshe.com/ko/reaction/1677607

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl chloroformateHCID 10387—
반응물Sodium HydroxideHCID 14798—
반응물1-Amino-2-methylpropylphosphonous acidHCID 16127403—
용매WaterHCID 962—
생성물1-Carbobenzyloxyamino-2-methylpropanephosphonous acidHCID 21325852—

반응 조건

온도0 °C

반응 단계

1-(diphenylmethylamino)-2-methylpropylphosphonous acid (12 g) was suspended in 100 mL of 48% hydrobromic acid, then heated at 100° C. for 2 hours until two distinct phases separated. The mixture was evaporated to dryness in vacuo, and the residue taken up in 100 mL of water. The aqueous solution was washed several times with ether to remove diphenylmethyl bromide and then evaporated to give an 80 mL solution of 1-amino-2-methylpropylphosphonous acid, a compound of formula (Xd). The solution of 1-amino-2-methylpropylphosphonous acid in 80 ml water was adjusted to pH 9.5 using 4 N NaOH, and the solution was cooled to 0° C. by an ice bath. Benzyl chloroformate (7.1 mL, 47 mmol) was added dropwise over 30 minutes and the resulting mixture was stirred for an additional 12 hours while the pH was maintained at pH 9-9.5 by periodic addition of 4 N NaOH. The reaction mixture was washed with ether (3×100 mL) to remove excess benzyl chloroformate. The aqueous solution was acidified using concentrated HCl to pH 1, then extracted by ethyl acetate (4×100 mL). The organic phase was dried over Na2SO4 and concentrated to afford 9.2 g of 1-(benzyloxycarbonylamino)-2-methylpropylphosphonous acid, as a white solid, which could be used in further reactions without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08008325B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-bb2bb2207c5c4ea98bef3908d25149dc
출처 메모uspto-grants-2011_08