Hydrochloric Acid → HCID 57429435、化合物

HRID 1640028ノート

反応式

HRID 1640028 の反応式
[CH3:1][C:2]1[C:3]([C:12]([OH:14])=[O:13])=[CH:4][C:5]2[O:10][CH2:9][CH2:8][O:7][C:6]=2[CH:11]=1.S(Cl)(Cl)=O.Cl.[CH2:20](OCC)[CH3:21]>C(O)C>[CH3:1][C:2]1[C:3]([C:12]([O:14][CH2:20][CH3:21])=[O:13])=[CH:4][C:5]2[O:10][CH2:9][CH2:8][O:7][C:6]=2[CH:11]=1

参加物

6

反応条件

温度
0 °C

実験手順

A mixture of 7-methyl-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylic acid (1.72 g, 8.8 mmol) in ethanol (100 mL) was cooled to 0° C. and stirred for 1 h prior to dropwise addition of thionyl chloride (3.9 mL, 53.2 mmol) over 1 h. After this time, the mixture was warmed to room temperature for 1 h, then transferred to an oil bath, and heated to 70° C. overnight. The mixture was then cooled to room temperature and 2 N hydrochloric acid (50 mL) added slowly followed by diethyl ether (50 mL). The aqueous layer was extracted twice with diethyl ether (50 mL), the combined organic layers washed with brine (100 mL), dried over magnesium sulfate, and concentrated under reduced pressure to afford ethyl 7-methyl-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylate (1.7 g, 89%) as a white solid: 1H NMR (500 MHz, CDCl3) δ 7.51 (s, 1H), 6.70 (s, 1H), 4.30 (q, J=7.0, 7.5 Hz, 2H), 4.26 (m, 4H), 2.49 (s, 3H), 1.36 (t, J=7.0, 7.5 Hz, 3H).

後処理

  1. temperatureAfter this time, the mixture was warmed to room temperature for 1 h
  2. customtransferred to an oil bath
  3. temperatureheated to 70° C. overnight
  4. temperatureThe mixture was then cooled to room temperature
  5. extractionThe aqueous layer was extracted twice with diethyl ether (50 mL)
  6. washthe combined organic layers washed with brine (100 mL)
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-f0eb801e6eb14382b49be7960e32cbf6
出典データセット
uspto-grants-2012_02
特許番号
US08110681B2

反応ノート

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