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3-(Bromomethyl)thiophene → 3-(Methoxyethoxyethoxymethyl)thiophene

HRID 981778
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HRID 981778 반응식
[CH3:1][O:2][CH2:3][CH2:4][O:5][CH:6]([CH3:8])[O-].[Na+].Br[CH2:11][C:12]1[CH:16]=[CH:15][S:14][CH:13]=1.C[O:18]CCOC(O)C>C(Cl)(Cl)(Cl)Cl>[CH3:1][O:2][CH2:3][CH2:4][O:5][CH2:6][CH2:8][O:18][CH2:11][C:12]1[CH:16]=[CH:15][S:14][CH:13]=1
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참가 물질

5

반응물 3

HCID 5207033-(Bromomethyl)thiopheneHCID 14367673HCID 14367673, 화합물HCID 88434596HCID 88434596, 화합물

생성물 1

HCID 570643253-(Methoxyethoxyethoxymethyl)thiophene수율 46%

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

A solution of sodium methoxyethoxyethoxide (29.6 g, 0.2 mol) in methoxyethoxyethanol (100 ml) was added to a solution of 3-(bromomethyl)thiophene (12.4 g, 0.07 mol) in carbon tetrachloride (25 ml) and the mixture heated under reflux for 12 hours. Work-up as described in Example 1 gave a crude oil which was distilled under reduced pressure to yield 3-(methoxyethoxyethoxymethyl)thiophene (7.0 g, 46%), B.p. 136°-138° C./10 mm. Hg. (Found: C, 56.0; H, 7.0; S, 15.1. Calculated for C10H16O3S: C, 55.5; H, 7.4; S, 14.8%); EI m/e Intensity (%): 216 (12 M+), 97 (100, C4H3S.CH2); δH(CDCl3): 6.96-7.17 (3H, m), 4.45 (2H, s), 3.50 (4H, m), 3.40 (4H, m) and 3.26 (3H, s); δ C(CDCl3): 58.3, 66.1, 69.2, 70.2, 70.4, 71.7, 121.7, 125.2, 126.7, 139.6 ppm.

후처리

  1. temperaturethe mixture heated
  2. temperatureunder reflux for 12 hours
  3. customgave a crude oil which
  4. distillationwas distilled under reduced pressure

출처 및 근거

ORD 기록
ord-b0f6c3e5a64f40ff9d43b1d1a67eda06
출처 데이터셋
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04992559

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