Potassium Hydroxide → HCID 57900438, Verbindung

HRID 628097Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 628097
[Br:1][C:2]1[CH:11]=[CH:10][C:9]2[O:8][CH2:7][C:6]3[CH:12]=[C:13]([C:15]([O:17]C)=[O:16])[S:14][C:5]=3[C:4]=2[CH:3]=1.[OH-].[K+]>O1CCCC1.O>[Br:1][C:2]1[CH:11]=[CH:10][C:9]2[O:8][CH2:7][C:6]3[CH:12]=[C:13]([C:15]([OH:17])=[O:16])[S:14][C:5]=3[C:4]=2[CH:3]=1

Komponenten

4

Versuchsvorschrift

To a suspension of methyl 8-bromo-4H-thieno[3,2-c]chromene-2-carboxylate 2 (2.64 g, 8.12 mmol, 1 equiv) in 4:1 tetrahydrofuran/water (80 mL) was added aqueous potassium hydroxide (24 mL, 24 mmol, 3.0 equiv, 1.0 M solution in water) at 24° C. After 15 hr, the tetrahydrofuran was removed in vacuo (<20 mm Hg). The resulting aqueous suspension was diluted with water until all the solids were dissolved. To the resulting solution was added concentrated hydrochloric acid until the solution reached pH=1. The resulting solids were collected by filtration and dried in vacuo (<1 mm Hg) to afford 3bp as a yellow solid (2.36 g, 93%). 1H NMR (500 MHz, CDCl3), δ: 13.28 (br s, 1H), 7.64 (d, J=2.4 Hz, 1H), 7.60 (s, 1H), 7.40 (dd, J=8.7, 2.4 Hz, 1H), 6.94 (d, J=8.7 Hz, 1H), 5.30 (s, 3H).

Aufarbeitung

  1. customthe tetrahydrofuran was removed in vacuo (<20 mm Hg)
  2. additionThe resulting aqueous suspension was diluted with water until all the solids
  3. dissolutionwere dissolved
  4. additionTo the resulting solution was added concentrated hydrochloric acid until the solution
  5. filtrationThe resulting solids were collected by filtration
  6. customdried in vacuo (<1 mm Hg)

Quellen und Nachweise

ORD-Eintrag
ord-d4d3f25ccc824f8a9d001232be1b6f6f
Quelldatensatz
uspto-grants-2016_04
Patentnummer
US09309265B2

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