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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 255963생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/255963

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물BromoetheneHCID 11641—
반응물MagnesiumHCID 5462224—
반응물(Hexadecyloxy) acetaldehydeHCID 14785848—
촉매1,1-DibromoethaneHCID 11201—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물1-(Hexadecyloxy)but-3-EN-2-OLHCID 1395907141.5%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04699990
출처 데이터셋uspto-grants-1987_10
ORD IDord-41414b2cf6584599ac72779c5a79dd96
출처 메모uspto-grants-1987_10