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HRID 21743作成日:2026年10月25日

N-alpha-Benzyloxycarbonyl-L-lysine → N2-[(Phenylmethoxy)carbonyl]-L-lysine tert-Butyl Ester

https://huagongshe.com/reaction/21743

反応式

関与物質

役割名称HCID仕込み量
反応物N-alpha-Benzyloxycarbonyl-L-lysineHCID 75172—
溶媒tert-Butyl acetateHCID 10908—
溶媒Perchloric AcidHCID 24247—
生成物N2-[(Phenylmethoxy)carbonyl]-L-lysine tert-Butyl EsterHCID 1107821972%

反応手順

Nα -(Benzyloxycarbonyl)-L-lysine (5.0 gm, 17.84 mmol) was dissolved in 268 ml of tert-butyl acetate containing 2.80 ml of perchloric acid (69-72% aqueous solution). The solution was stirred for 2 days at room temperature and then was extracted with water (3×200 ml). The combined aqueous layers were adjusted to pH 10 with 50% sodium hydroxide. The aqueous solution was then extracted with ethyl acetate (3×200 ml) and the organic layers dried over MgSO4. After filtration to remove MgSO4, the solvent was removed by evaporation at reduced pressure to provide Nα -(benzyloxycarbonyl)-L-lysine tert-butyl ester as a clear oil (2.16 gm, 36%). 1H NMR (CDCl3) 1.35 (s,9H), 1.40-2.0 (m,6H), 2.60 (t,2H), 4.10 (m, 1H), 4.98 (s,2H), 5.29 (bs,1H), 7.35 (s,5H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05424447
出典データセットuspto-grants-1995_06
ORD IDord-8224666d4e8f467c8cbd4d16ff05bd05
出典メモuspto-grants-1995_06