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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1876299생성일: 2026년 10월 25일

2-Methyl-2-butene → (S)-4-acetoxypent-2-ynoic acid

https://huagongshe.com/reaction/1876299

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-2-buteneHCID 10553—
반응물(S)-4-formylbut-3-yn-2-yl acetateHCID 11499231—
반응물Sodium ChloriteHCID 23668197—
용매WaterHCID 962—
용매tert-ButanolHCID 6386—
생성물(S)-4-acetoxypent-2-ynoic acidHCID 59552181100.6%

반응 단계

To a solution of 9 (133 mg, 0.949 mmol) and 2-methyl-2-butene (1.20 mL, 14.2 mmol) in tBuOH (1.9 mL) was added the mixture of NaClO2 (257 mg, 2.84 mmol) and NaH2PO4 (393 mg, 2.84 mmol) in H2O (1.9 mL) at 23° C. The resulting mixture was stirred for 20 min at the same temperature and quenched by 1 N aqueous HCl (3 mL) at 0° C. The mixture was poured into a separatory funnel and diluted with EtOAc (3 mL). The layers were separated and the aqueous layer was extracted with EtOAc (3×4 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated in vacuo. Purification of the residue via flash chromatography (silica gel 15 mL; 50→100% EtOAc in hexanes containing 1.0% acetic acid) afforded acid 10 (149 mg, quantitative yield) as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08309599B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-388c0eb8c23f4f9eacdd01bceaa2f18c
출처 메모uspto-grants-2012_11