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Triethylamine → HCID 117761061, 화합물

HRID 1748420
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HRID 1748420 반응식
Br[CH2:2][C:3]1[CH:8]=[C:7]([Br:9])[CH:6]=[C:5]([Br:10])[C:4]=1[OH:11].N[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[SH:19].C([N:22](CC)CC)C>C1COCC1>[NH2:22][S:19][C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=1[CH2:2][C:3]1[CH:8]=[C:7]([Br:9])[CH:6]=[C:5]([Br:10])[C:4]=1[OH:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 87132-AminothiophenolHCID 6221772,4-Dibromo-6-(bromomethyl)phenol

생성물 1

HCID 117761061HCID 117761061, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of 2-(bromomethyl)-4,6-dibromophenol (1.48 g, 4.3 mmol) in THF (20 mL) was added dropwise to a solution of 2-Aminothiophenol (0.54 g, 4.3 mmol) and triethylamine (0.60 mL) in THF (20 mL) and stirred at room temperature for 12 hours. A solid had formed and was filtered out followed by removal of the solvent in vacuum. The crude product was dissolved in dichloromethane, washed with saturated NaCl solution and dried over MgSO4. The product was obtained as a yellow oil in a quantitative yield.

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후처리

  1. customA solid had formed
  2. filtrationwas filtered out
  3. customfollowed by removal of the solvent in vacuum
  4. dissolutionThe crude product was dissolved in dichloromethane
  5. washwashed with saturated NaCl solution
  6. dry with materialdried over MgSO4
  7. customThe product was obtained as a yellow oil in a quantitative yield

출처 및 근거

ORD 기록
ord-fd9e5684b8d14df18d4376d0db64dd4d
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09150676B2

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