Hydrochloric Acid → [3-(2-Hydroxy-1-methylethyl)-4-nitrophenyl]phenylmethanone

HRID 2357145노트

반응식

HRID 2357145 반응식
[OH:1][CH2:2][CH:3]([C:5]1[CH:6]=[C:7]([C:14]2([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)OCCC[O:15]2)[CH:8]=[CH:9][C:10]=1[N+:11]([O-:13])=[O:12])[CH3:4].Cl>C(O)C.O>[C:14]([C:7]1[CH:8]=[CH:9][C:10]([N+:11]([O-:13])=[O:12])=[C:5]([CH:3]([CH3:4])[CH2:2][OH:1])[CH:6]=1)(=[O:15])[C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 59386295HCID 59386295, 화합물

생성물 1

HCID 59386296[3-(2-Hydroxy-1-methylethyl)-4-nitrophenyl]phenylmethanone수율 91%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매2회

실험 절차

To a solution of 2-(3-(2-hydroxy-1-methylethyl)-4-nitrophenyl)-2-phenyl-1,3-dioxane (18) (23.6 g; approx. 69 mmol) in ethanol (350 mL) was added water (70 mL) under vigorous stirring. Concentrated hydrochloric acid (about 12 N aqueous solution, 35 mL) was then added drop wise. The reaction mixture was stirred at ambient temperature for 4 hours, diluted with water and extracted with ethyl acetate. The organic phase was successively washed with an aqueous, saturated solution of NaHCO3 and with water. The organic phase was then concentrated in vacuo and seeded with crystals of the product 4f to provide a yellow solid. Finally, the powdered solid was washed with hexane and air dried to yield 17.83 g (62.5 mmol, 91%) of a yellow powder. 1H NMR (250 MHz, DMSO-d6) δ 7.91-7.52 (m, 8H, arom.), 4.75 (br. s., 1H, OH), 3.53 (d, 2H, α-CH2), 3.23 (sextet, 1H, β-CH), 1.24 (d, 3H, γ-CH3).

후처리

  1. extractionextracted with ethyl acetate
  2. washThe organic phase was successively washed with an aqueous, saturated solution of NaHCO3
  3. concentrationThe organic phase was then concentrated in vacuo
  4. customto provide a yellow solid
  5. washFinally, the powdered solid was washed with hexane and air
  6. customdried

출처 및 근거

ORD 기록
ord-0adb48d2fe844b3ebedf6f2d406fc6f8
출처 데이터셋
uspto-grants-2010_07
특허 번호
US07759513B2

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