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HRID 1283846作成日:2026年10月27日

Triethylamine → 1-((Tert-butoxy)carbonyl)pyrrolidine-3-carboxylic acid

https://huagongshe.com/reaction/1283846

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物AzideHCID 33558—
反応物Carbonazidic acid, 1,1-dimethylethyl esterHCID 61256—
反応物3-Pyrrolidinecarboxylic acidHCID 3034645—
反応物1-benzylpyrrolidine-3-carboxylic AcidHCID 4617348—
触媒PalladiumHCID 23938—
溶媒Acetic AcidHCID 176—
溶媒N,N-Dimethylformamide--water (1/1)HCID 21962138—
生成物1-((Tert-butoxy)carbonyl)pyrrolidine-3-carboxylic acidHCID 2760529—

反応手順

A solution of 205 g. (1 mol.) of N-benzylpyrrolidine-3-carboxylic acid (CA, 64 14173d) is dissolved in glacial acetic acid (1 l.) and hydrogenated in the presence of 40 g. of 10% palladium on charcoal until no more starting material is detected by TLC. The catalyst is filtered off and the filtrate is concentrated to dryness in vacuo. The residual 3-pyrrolidine carboxylic acid is dissolved in a mixture of DMF-H2O (2:1) (2 liters), triethylamine (1 mol.), t-butoxycarbonyl azide (1.5 mol.) is added and the mixture is stirred at room temperature for two days. Periodically the pH is tested with pH paper, and after twenty-four hours more azide (0.5 mol.) is added. The solvent is concentrated in vacuo to remove the DMF, the aqueous phase is acidified with citric acid (to pH 2-3) and extracted with ethyl acetate. The organic phase is concentrated to dryness in vacuo to yield the product 1-(t-butyloxycarbonyl)-3-pyrrolidinecarboxylic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03976660
出典データセットuspto-grants-1976_08
ORD IDord-dd959544468b462a8ddaf8774f1400b1
出典メモuspto-grants-1976_08