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HRID 255963作成日:2026年10月27日

Hydrochloric Acid → 1-(Hexadecyloxy)but-3-EN-2-OL

https://huagongshe.com/reaction/255963

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物BromoetheneHCID 11641—
反応物MagnesiumHCID 5462224—
反応物(Hexadecyloxy) acetaldehydeHCID 14785848—
触媒1,1-DibromoethaneHCID 11201—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物1-(Hexadecyloxy)but-3-EN-2-OLHCID 1395907141.5%

反応条件

温度0 °C

反応手順

To a stirring mixture of 5.67 g of magnesium in 25 ml of tetrahydrofuran was added 10 drops of dibromoethane as an initiator. After the reaction began another 100 ml of tetrahydrofuran was added followed by the dropwise addition of a solution of 49.85 g of vinyl bromide in 250 ml of tetrahydrofuran at a rate to maintain reflux. After all of the magnesium had reacted, the solution was cooled to 0° C. and a solution of 44.2 g of (hexadecyloxy) acetaldehyde, prepared by the procedure of Example 3, in 175 ml of ether was added dropwise over 1/2 hour. After 1 hour at room temperature dilute hydrochloric acid was added. The tetrahydrofuran was removed and the residue was extracted with ether. The ether layer was washed with brine, dried and the solvent removed. The residue was purified by HPLC [hexane: ether (9:1), two columns, two passes] giving an oil which was distilled via a Kugelrohr apparatus (185°-190° C., 0.2 mm) giving a colorles oil which solidified on standing to give 20.17 g of the desired compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04699990
出典データセットuspto-grants-1987_10
ORD IDord-41414b2cf6584599ac72779c5a79dd96
出典メモuspto-grants-1987_10