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HRID 1803202생성일: 2026년 10월 27일

1-Chloro-4-iodobutane → 6-Chloro-2-(4-isopropoxyphenyl)hexanoic acid

https://huagongshe.com/reaction/1803202

반응식

참여 물질

역할이름HCID투입량
반응물1-Chloro-4-iodobutaneHCID 82527—
반응물Benzeneacetic acid, 4-(1-methylethoxy)-HCID 799528—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
생성물6-Chloro-2-(4-isopropoxyphenyl)hexanoic acidHCID 5811009337.6%

반응 단계

Step AV (1): 2-(4-Isopropoxyphenyl)acetic acid (7.7 g, 39.6 mmol, reference G. Solladie et al. Tetrahedron (2003), 59, 3315) was deprotonated with NaHMDS (2.0 M in THF, 39.5 mL, 79 mmol) and reacted with 1-chloro-4-iodobutane (10.8 g, 49.6 mmol) using a procedure analogous to Step AC (1) to afford 6-chloro-2-(4-isopropoxyphenyl)hexanoic acid (4.24 g, 37% yield) as a clear viscous oil. LC-MS (M−H)− 193.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08349880B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-c1e30653e83043e8b52e904d30e0a7fa
출처 메모uspto-grants-2013_01