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HRID 1419951作成日:2026年10月27日

Boron tribromide → (trans)-N-[[2-[3-(2-Propenyloxy)phenyl]cyclopropyl]methyl]butanamide

https://huagongshe.com/reaction/1419951

反応式

関与物質

役割名称HCID仕込み量
反応物Boron tribromideHCID 25134—
反応物(trans)-N-[[2-(3-methoxyphenyl)cyclopropyl]methyl]butanamideHCID 15860309—
反応物(trans)-N-[[2-(3-Hydroxyphenyl)cyclopropyl]methyl]butanamideHCID 70274674—
溶媒DichloromethaneHCID 6344—
生成物(trans)-N-[[2-[3-(2-Propenyloxy)phenyl]cyclopropyl]methyl]butanamideHCID 1586031375%

反応手順

(trans)-N-[[2-(3-Hydroxyphenyl)cyclopropyl]methyl]butanamide: To a stirred solution of (trans)-N-[[2-(3-methoxyphenyl)cyclopropyl]methyl]butanamide (3.50 g, 14.2 mmol) in dichloromethane (50 mL) at -78° C. was added BBr3 (28.4 mL, 1N in CH2Cl2, 28.4 mmol) dropwise. After addition was complete, the cooling bath was removed and stirring was continued for 18 h. The solution was poured over ice/H2O(100 mL) and extracted with 2.5 N NaOH. The basic extracts were combined, washed with dichloromethane, and acidified (conc. HCl). The acidic solution was extracted with dichloromethane, the organics were combined, washed with brine, dried (MgSO4), and concentrated to afford 2.49 g (75%) of the title compound: 1H NMR (300 MHz, DMSO-d6) δ 0.72-0.84 (m, 5H), 1.09-1.15 (m, 1H), 1.42-1.54 (m, 2H), 1.63-1.69 (m, 1H), 2.02 (t, J=5.0 Hz, 2H), 2.99-3.11 (m, 2H), 6.39-6.50 (m, 3H), 6.98 (t, J=7.8 Hz, 1H), 7.91 (s, 1H), 9.19 (br s, 1H); IR (NaCl Film) 3300, 2964, 1642, 1585, 1542, 1466 cm-1 ; MS (isobutane-DCI) m/e 233; Analysis calc'd for C14H19NO2.0.1 H2O: C, 71.52; H, 8.23; N, 5.96; found: C, 71.53; H, 8.32; N, 5.92.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05889031
出典データセットuspto-grants-1999_03
ORD IDord-76a393d8f83b490e9ba8aacd4ffe6e65
出典メモuspto-grants-1999_03