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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbon Tetrachloride | HCID 5943 | — |
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | Ethyl 14-hydroxy-2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenoate | HCID 54363154 | — |
| 생성물 | Ethyl 14-chloro-2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05399724 |
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| 출처 데이터셋 | uspto-grants-1995_03 |
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| ORD ID | ord-9e46dad88ccd4f24a7f5505f1f48b3c8 |
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| 출처 메모 | uspto-grants-1995_03 |
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