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HRID 1283846생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1283846

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물AzideHCID 33558—
반응물Carbonazidic acid, 1,1-dimethylethyl esterHCID 61256—
반응물3-Pyrrolidinecarboxylic acidHCID 3034645—
반응물1-benzylpyrrolidine-3-carboxylic AcidHCID 4617348—
촉매PalladiumHCID 23938—
용매Acetic AcidHCID 176—
용매N,N-Dimethylformamide--water (1/1)HCID 21962138—
생성물1-((Tert-butoxy)carbonyl)pyrrolidine-3-carboxylic acidHCID 2760529—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03976660
출처 데이터셋uspto-grants-1976_08
ORD IDord-dd959544468b462a8ddaf8774f1400b1
출처 메모uspto-grants-1976_08