Triethylamine → 1-Ethyl-3-(4,5,6,7-tetrahydrobenzo[b]thien-4-yl)thiourea

HRID 1701202ノート

反応式

HRID 1701202 の反応式
Cl.[S:2]1[CH:6]=[CH:5][C:4]2[CH:7]([NH2:11])[CH2:8][CH2:9][CH2:10][C:3]1=2.C(N(CC)CC)C.[CH2:19]([N:21]=[C:22]=[S:23])[CH3:20]>O1CCCC1>[CH2:19]([NH:21][C:22]([NH:11][CH:7]1[C:4]2[CH:5]=[CH:6][S:2][C:3]=2[CH2:10][CH2:9][CH2:8]1)=[S:23])[CH3:20]

参加物

5

反応条件

温度
50 °C

実験手順

A sample of 9.48 grams of 4,5,6,7-tetrahydrobenzo[b]thiophen-4-amine hydrochloride is stirred in 100 ml. of dry tetrahydrofuran, and 6.06 grams of triethylamine is added. After stirring for 15 to 30 minutes, 5.23 grams of ethyl isothiocyanate in 20 ml. of dry tetrahydrofuran is added dropwise, and the mixture is heated for 2 hours at 50° C. The mixture is cooled and filtered, and the filter cake is washed with hexane. The filtrate is evaporated to dryness and poured on ice. The oil is extracted with ether, and the extract is washed with 1 N sulfuric acid, water, and saturated sodium bicarbonate solution. The ether extract is dried and evaporated to dryness to afford an oil. This oil crystallizes in ether to afford 1-ethyl-3-(4,5,6,7-tetrahydrobenzo[b]thien-4-yl)thiourea, melting point 106° C. to 112° C.

後処理

  1. temperatureThe mixture is cooled
  2. filtrationfiltered
  3. washthe filter cake is washed with hexane
  4. customThe filtrate is evaporated to dryness
  5. additionpoured on ice
  6. extractionThe oil is extracted with ether
  7. washthe extract is washed with 1 N sulfuric acid, water, and saturated sodium bicarbonate solution
  8. extractionThe ether extract
  9. customis dried
  10. customevaporated to dryness
  11. customto afford an oil
  12. customThis oil crystallizes in ether

出典と根拠

ORDレコード
ord-a1393d7a6d0c4b0296b8018979af8bb3
出典データセット
uspto-grants-1980_03
特許番号
US04191830

反応ノート

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