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HRID 2883作成日:2026年10月23日

(2S,4R)-N-t-Butoxycarbonyl-4-methyl glutamic acid → 2S,4R-4-Methylglutamate

https://huagongshe.com/ja/reaction/2883

反応式

関与物質

役割名称HCID仕込み量
反応物(2S,4R)-N-t-Butoxycarbonyl-4-methyl glutamic acidHCID 54118427—
溶媒Trifluoroacetic acid methylene chlorideHCID 21863450—
生成物2S,4R-4-MethylglutamateHCID 95883—

反応手順

The Boc-protected diacid, (2S, 4R)-N-t-butoxycarbonyl- 4-methyl glutamic acid, was subjected to a mixture of trifluoroacetic acid:methylene chloride (40:60, 100 mL) for 3 hr at room temperature. The volatiles were removed in vacuo and the residue was azeotroped with toluene (50 mL). Water (150 mL) was added and the aqueous phase extracted with a 5% solution of trioctylamine in chloroform (3 x 200 mL). The combined organic phases were washed with water (50 mL) and the combined aqueous phases evaporated by being placed on a lyophilizer for 48 hr to give the product (4.6 g, 66% in two steps) as a white foam which was recrystallized in acetone and water. mp=169°-170° C., 1H NMR (200 MHz, D2O): δ 3.80 (dd, J=7.3, 7.3 Hz, 1H), 2.55 (m, 1H), 2.15 (ddd, J=14.7, 8.7, 6.6 Hz, 1H), 1.75 (ddd, J=14.6, 7.4, 5.4 Hz, 1H), 1.05 (d, J=7.0 Hz, 3H). Anal. Calculated for C6H11NO4 : C, 44.71; H, 6.88; N, 8.69. Found: C, 44.59; H, 6.85; N, 8.61.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731348
出典データセットuspto-grants-1998_03
ORD IDord-cc72150513eb4fa69899ef3b1e23e777
出典メモuspto-grants-1998_03