(Diethylamino)sulfur trifluoride → HCID 54007397、化合物

HRID 2232624ノート

反応式

HRID 2232624 の反応式
C(N(S(F)(F)[F:7])CC)C.[CH3:10][O:11][C:12]([C:14]1([CH:17](O)[CH2:18][CH2:19][CH2:20][CH2:21][O:22][C:23]2[CH:28]=[CH:27][C:26]([Cl:29])=[CH:25][CH:24]=2)[CH2:16][O:15]1)=[O:13]>C(Cl)Cl>[CH3:10][O:11][C:12]([C:14]1([CH:17]([F:7])[CH2:18][CH2:19][CH2:20][CH2:21][O:22][C:23]2[CH:28]=[CH:27][C:26]([Cl:29])=[CH:25][CH:24]=2)[CH2:16][O:15]1)=[O:13]

参加物

4

反応条件

温度
-78 °C

実験手順

To a solution of 967 mg (6 mmol, 733 μl) of diethylaminosulfur trifluoride in 25 ml of methylene chloride cooled to -78° C. under a nitrogen atmosphere is added dropwise a solution of 945 mg (3 mmol) of 2-[5-(4-chlorophenoxy)-1-hydroxypentyl]-2-oxiranecarboxylic acid methyl ester (isomer A) in 25 ml of methylene chloride over 30 minutes. The mixture is stirred at -78° C. for 30 minutes and then is allowed to come to room temperature. The mixture is stirred at room temperature for 1.5 hours, is quenched with brine and is extracted with ethyl ether. The combined ethereal extracts are dried over magnesium sulfate, filtered and rotoevaporated to give a crude solid. Trituration with cyclohexane:isopropyl ether and subsequent high vacuum drying affords 597 mg of the title compound (isomer A) (Rf 0.45 in hexane:ethyl ether (1:1)): m.p. 76°-78° C.; IR (KBr) γ1740, 1497, 1257, 832 and 758 cm-1 ; NMR (CDCl3) δ1.54-2.02 (6H, m), 3.10 (1H, dd, J=3, 6 Hz), 3.18 (1H, d, J=6 Hz), 3.80 (3H, s), 3.96 (2H, t, J=7 Hz), 5.19 (1H, ddd, JHF = 48 Hz, 10, 3 Hz), 6.85 (2H, d, J=7 Hz) and 7.27 (2H, d, J=7 Hz).

後処理

  1. customto come to room temperature
  2. stirringThe mixture is stirred at room temperature for 1.5 hours
  3. customis quenched with brine
  4. extractionis extracted with ethyl ether
  5. dry with materialThe combined ethereal extracts are dried over magnesium sulfate
  6. filtrationfiltered
  7. customto give a crude solid
  8. dry with materialTrituration with cyclohexane:isopropyl ether and subsequent high vacuum drying

出典と根拠

ORDレコード
ord-15f340b62f964349adf4e7d03c2b07ea
出典データセット
uspto-grants-1988_11
特許番号
US04788304

反応ノート

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