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Hydrogen Bromide → HCID 178515467, 화합물

HRID 428627
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HRID 428627 반응식
C[O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]([CH2:13][C:14]1[N:15]=[CH:16][NH:17][CH:18]=1)[CH2:8][CH2:7][CH2:6]2.Br.[OH-].[NH4+]>O>[NH:17]1[CH:18]=[C:14]([CH2:13][CH:9]2[CH2:8][CH2:7][CH2:6][C:5]3[CH:4]=[C:3]([OH:2])[CH:12]=[CH:11][C:10]2=3)[N:15]=[CH:16]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 260Hydrogen BromideHCID 14923Ammonium HydroxideHCID 178487147HCID 178487147, 화합물

생성물 1

HCID 178515467HCID 178515467, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A stirred mixture of 4-(6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ylmethyl)-1H-imidazole (220 mg) and 48% hydrobromic acid (11 ml) is heated under reflux for one hour. The cooled reaction mixture is poured into water and is made basic with ammonium hydroxide solution. The product is extracted into ethyl acetate which is washed with water, dried with sodium sulfate and evaporated to dryness. The crude product is converted to its hydrochloride salt in ethyl acetate. The yield is 130 mg, m.p. 200-205° C.

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후처리

  1. temperatureis heated
  2. temperatureunder reflux for one hour
  3. customThe cooled reaction mixture
  4. extractionThe product is extracted into ethyl acetate which
  5. washis washed with water
  6. dry with materialdried with sodium sulfate
  7. customevaporated to dryness

출처 및 근거

ORD 기록
ord-4ee20560ea90443bb14d823bc4160928
출처 데이터셋
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06313311B1

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