تفاعل #1869171

ord-b3178f60b4774d0b9e3efc65f3fe44ff

معادلة التفاعل

COc1cc2c(cc1O)CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
2-Methoxyestrone
COc1cc2c(cc1O)CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
2-methoxyestrone
Cl
HCl
NN.O
Hydrazine hydrate
[K+].[OH-]
KOH
COc1cc2c(cc1O)CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Compound 4
COc1cc2c(cc1O)CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
2-methoxyestrone
COc1cc2c(cc1O)CC[C@@H]1[C@@H]2CC[C@]2(C)CCC[C@@H]12
Compound 7
المردود 72.0%
COc1cc2c(cc1O)CC[C@@H]1[C@@H]2CC[C@]2(C)CCC[C@@H]12
2-Methoxyestra-1,3,5(10)-triene-3-ol
المردود 72.0%

المذيبات

ظروف التفاعل

درجة الحرارة
130°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction was cooled to 70° C.
  2. 2
    درجة الحرارةthe reaction was heated at 200° C. for 1 h
  3. 3
    درجة الحرارةThe mixture was cooled to room temperature
  4. 4
    workup.ADDITIONwas added
  5. 5
    ترشيحThe resulting solid was filtered off
  6. 6
    workup.DISSOLUTIONThe solid was dissolved in acetone
  7. 7
    أخرىwhich was then evaporated

الإجراء التجريبي

2-Methoxyestrone (Scheme 1, Compound 4) (450 mg, 1.5 mmol) was suspended in ethylene glycol (10 mL) and n-butanol (2 mL). Hydrazine hydrate (0.145 mL, 3 mmol) was added and the mixture was heated to 130° C. for 1 h. The reaction was cooled to 70° C., KOH (253 mg, 4.5 mmol) was added, then the reaction was heated at 200° C. for 1 h. The mixture was cooled to room temperature, poured into ice and HCl (6N, 6 mL) was added. The resulting solid was filtered off. The solid was dissolved in acetone, which was then evaporated to give a product (Scheme 1, Compound 7) (310 mg, 72% yield). 1H NMR (300 MHz, CDCl3) δ 6.93 (1H, s, aromatic), 6.75 (1H, s, aromatic), 5.35 (1H, s, phenol), 3.95 (3H, s, methoxy), 2.95 (2H, dd, J=5.0, 3.0 Hz), 2.25 (2H, m,), 1.95 (2H, m), 1.95-1.05 (11H, m), 0.8 (3H, s)

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07498322B2uspto-grants-2009_03