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HRID 2167158作成日:2026年10月27日

Iodoethane → 1-(1-Methoxyisopropoxy)pent-2-yne

https://huagongshe.com/reaction/2167158

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物IsopreneHCID 6557—
反応物3-(1-Methoxy-1-methylethoxy)propyneHCID 3017891—
反応物HCID 178506930HCID 178506930—
溶媒HexaneHCID 8058—
生成物1-(1-Methoxyisopropoxy)pent-2-yneHCID 3019831120.6%

反応手順

0.89 g (127 mmol) of granulated lithium were added within 15 minutes to 100 ml (4 mol) of liquid ammonia at −37° C. The mixture was stirred until no more lithium floated (after approximately 15 minutes). A dark blue solution of lithium in liquid ammonia was obtained. 5.94 g (86.3 mmol) of isoprene were added portion wise within 30 minutes. The end of the formation of LiNH2 could be recognized by the de-coloration of the reaction mixture and 10.69 g (70.1 mmol) of 3-(1-methoxy-1-methyl-ethoxy)-propyne were added to the reaction mixture at −37° C. within 30 minutes. The reaction mixture was held at −37° C. for about 1 hour. Ethyl iodide (20.05 g, 126 mmol) was added with a dropping funnel to the reaction mixture within 30 minutes. The reaction mixture was subsequently stirred for 1 hour. n-Hexane (100 ml) was added to the reaction mixture and the liquid ammonia was evaporated under normal pressure within 1.5 hours. Water (50 ml) was added to the reaction mixture at 22° C., and the mixture was vigorously stirred until all salt was dissolved. The water layer was extracted twice with 50 ml n-hexane. The organic layer was dried over 5 g of anhydrous sodium sulfate. The solution was concentrated under reduced pressure (40° C., 60 mbar) and the crude product was analyzed by GC. Crude 1-(1-methoxy-1-methyl-ethoxy)-pent-2-yne (13.21 g) were obtained with a purity of 72.95% (88.0% yield based on 3-(1-methoxy-1-methyl-ethoxy)-propyne).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09045404B2
出典データセットuspto-grants-2015_06
ORD IDord-665dd9e7e7254d98bdd22c491de46dd7
出典メモuspto-grants-2015_06