3-(Bromomethyl)thiophene → HCID 54352789, compound

HRID 981777Notes

Reaction equation

HRID 981777 reaction equation
Br[CH2:2][C:3]1[CH:7]=[CH:6][S:5][CH:4]=1.[CH3:8][O:9][CH:10]([CH3:12])[O-].[Na+].C[O:15]C(O)C>C(Cl)(Cl)(Cl)Cl>[CH3:8][O:9][CH2:10][CH2:12][O:15][CH2:2][C:3]1[CH:7]=[CH:6][S:5][CH:4]=1

Participants

5

Procedure

A solution of 3(bromomethyl)thiophene (6.2 g, 0.035 mol) in carbon tetrachloride (25 ml) was added to a solution of sodium methoxyethoxide (8.9 g, 0.09 mol) in methoxyethanol (90 ml) and the mixture was heated under reflux for 2 hours. After cooling to room temperature, the solvent mixture was removed under reduced pressure and the resultant oil was dissolved in dichloromethane (100 ml), extracted with distilled water (2×100 ml) and dried over potassium carbonate. After removal of the solvent, the crude oil was distilled under reduced pressure to yield 3-(methoxyethoxymethyl)thiophene (3.0 g, 50%), B.p. 100°-101° C./10 mm Hg. (Found: C, 55.0; H, 6.3; S, 17.6. Calculated for C8H12O2S: C, 55.8; H, 7.0; S, 18.6%); EI m/e Intensity (%): 172 (5, M+), 97 (12, C4H3S.CH2); δH(CDCl3): 7.05-7.24 (3H, m), 4.53 (2H, s), 3.54 (4H, m) and 3.34 (3H, s); δC(CDCl3): 59.6, 67.0, 69.7, 72.5, 123.4, 126.5, 127.9, 140.0 ppm.

Workup

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 2 hours
  3. customthe solvent mixture was removed under reduced pressure
  4. dissolutionthe resultant oil was dissolved in dichloromethane (100 ml)
  5. extractionextracted with distilled water (2×100 ml)
  6. dry with materialdried over potassium carbonate
  7. customAfter removal of the solvent
  8. distillationthe crude oil was distilled under reduced pressure

Sources & evidence

ORD record
ord-ef8c16096a8a43afb7fd31843f0a0a00
Source dataset
uspto-grants-1991_02
Patent number
US04992559

Reaction notes

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