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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1609346생성일: 2026년 10월 26일

Carbon Tetrachloride → Ethyl 14-chloro-2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenoate

https://huagongshe.com/reaction/1609346

반응식

참여 물질

역할이름HCID투입량
반응물Carbon TetrachlorideHCID 5943—
반응물HexaneHCID 8058—
반응물TriphenylphosphineHCID 11776—
반응물Ethyl 14-hydroxy-2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenoateHCID 54363154—
생성물Ethyl 14-chloro-2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenoateHCID 54546229—

반응 단계

To a solution of ethyl 14-hydroxy-2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenoate (713 mg, 2.03 mmol) in dry carbon tetrachloride (2 ml) was added triphenylphosphine (787 mg, 3.00 mmol), and the mixture was heated under reflux with stirring for 2 hours. After confirmation of disappearance of the starting material, the mixture was cooled to room temperature, and n-hexane was added thereto. Insoluble triphenylphosphine oxide was filtered and washed with n-hexane. The liltrate and the washing were combined and condensed. The resultant residue was added to a small amount of n-hexane, filtered, and washed to remove the residual triphenylphosphine oxide. The filtrate and the washing were combined and condensed to give as a residue the aimed ethyl 14-chloro-2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenoate. The product was used in the subsequent reaction without purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05399724
출처 데이터셋uspto-grants-1995_03
ORD IDord-9e46dad88ccd4f24a7f5505f1f48b3c8
출처 메모uspto-grants-1995_03