2-sec-Butylphenol → Fenobucarb

HRID 54028

반응식

HRID 54028 반응식
[CH:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[OH:11])([CH2:3][CH3:4])[CH3:2].CCN(CC)CC.[CH3:19][NH:20][C:21](=S)[OH:22]>C(#N)C>[CH3:19][NH:20][C:21](=[O:22])[O:11][C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=1[CH:1]([CH2:3][CH3:4])[CH3:2]

참가 물질

5

반응물 3

HCID 69842-sec-ButylphenolHCID 8471TriethylamineHCID 178486072HCID 178486072, 화합물

생성물 1

HCID 19588Fenobucarb

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a solution of 2-Sec. butylphenol (1.5 g, 0.01 mole) 0.2 ml of Et3N was added under stirring. S-methyl ester of N-methylcarbamothioic acid (1.05 g, 0.01 mole) in acetonitrile (10ml) was added dropwise over a period of 4 hrs, keeping reflux temperature. After 30 hr, acetonitrile was evaporated under vacuum. The residue was taken in dichloromethane (25 ml), washed with water and a 5% cold NaOH solution, followed by water and brine and dried over sodium sulphate. After removal of the solvent, the liquid residue obtained was further purified by distillation to give 2-Sec. butylphenyl N-methylcarbamate of the formula VI; IR: 3329 (N--H), 1730 (--COO), 1535, 1490 and 750 (aromatic); PMR (CdCl3, 90 MHz): 0.81 (3H, 1, primary methyl of side chain), 1.18 (3H, d, J=7 Hz, secondary/methyl of side chain), 1.58 (2H, m, methylene protons of side chain), 2.88 (4H, doublet overlapping a multiplet, NH--CH3 and benzylic proton), 4.97 (1H, br s, N H) and 6.95 to 7.25 (4H, m, aromatic).

후처리

  1. temperaturekeeping reflux temperature
  2. customacetonitrile was evaporated under vacuum
  3. washwashed with water
  4. dry with materialdried over sodium sulphate
  5. customAfter removal of the solvent
  6. customthe liquid residue obtained
  7. distillationwas further purified by distillation

출처 및 근거

ORD 기록
ord-7f50eba81d05416bb90b54131e3609c7
출처 데이터셋
uspto-grants-1997_04
특허 번호
US05621132

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