2-Phenylacetophenone → 4-(2-Oxo-2-phenylethyl)benzene-1-sulfonamide

HRID 343074ノート

反応式

HRID 343074 の反応式
Cl[S:2]([OH:5])(=O)=[O:3].[C:6]1([C:12]([CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[O:13])[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[NH4+:21].[OH-]>CC(C)=O>[NH2:21][S:2]([C:18]1[CH:17]=[CH:16][C:15]([CH2:14][C:12]([C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=2)=[O:13])=[CH:20][CH:19]=1)(=[O:5])=[O:3]

参加物

5

反応物 3

HCID 99482-PhenylacetophenoneHCID 14923Ammonium HydroxideHCID 24638Chlorosulfonic acid

生成物 1

HCID 222857924-(2-Oxo-2-phenylethyl)benzene-1-sulfonamide収率 29%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

Chlorosulfonic acid (1781 g, 1018 mL, 15.29 mol) was treated portionwise with deoxybenzoin (400 g, 2.04 mol) at such a rate that the internal temperature was maintained between 5° and 15° C. The mixture was warmed to room temperature and maintained at that temperature for an additional 14 hours. The mixture was poured cautiously into ice water. The crude sulfonyl chloride was filtered and added portionwise to a solution of acetone (600 mL) and concentrated NH4OH (551 mL, 8.15 mol), yielding a pale yellow suspension. The crude precipitate was collected by vacuum filtration, and triturated with boiling acetone (1.5 L). Filtration afforded 2-[4-aminosulfonylphenyl]-1-phenyl-ethan-1-one (162 g, 29%) as an off-white powder: 1H NMR (DMSO-d6, 300 MHz) 8.05 (d, J=7.25 Hz, 2H), 7.76 (d, J=8.26 Hz, 2H), 7.65 (t, J=7.85 Hz, 1H), 7.54 (t, J=7.85 Hz, 2H), 7.44 (d, J=8.26, 2H), 7.30 (br s, 2H), 4.52 (s, 2H).

後処理

  1. temperaturewas maintained between 5° and 15° C
  2. temperaturemaintained at that temperature for an additional 14 hours
  3. filtrationThe crude sulfonyl chloride was filtered
  4. customyielding a pale yellow suspension
  5. filtrationThe crude precipitate was collected by vacuum filtration
  6. customtriturated with boiling acetone (1.5 L)
  7. filtrationFiltration

出典と根拠

ORDレコード
ord-4b84169acae64933a2ca783eddbe44b2
出典データセット
uspto-grants-1999_01
特許番号
US05859257

反応ノート

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