تفاعل #1929035

ord-7e3629f0375b4c91bc4c57b706ae2f1c

معادلة التفاعل

[Br-].c1ccc(-[s+]2c3ccccc3c3ccccc32)cc1
5-phenyl-5H-dibenzo[b,d]thiophenium bromide
CC(=O)OC(C)C(F)(F)C(F)(F)S(=O)(=O)[O-].OC12CC3CC(CC(C3)C1)C2.[Na]
3-hydroxyadamantane acetoxy-1,1,2,2-tetrafluorobutane-1-sulfonate sodium
O
water
CC(OC(=O)CC12CC3CC(CC(O)(C3)C1)C2)C(F)(F)C(F)(F)S(=O)(=O)[O-].c1ccc(-[s+]2c3ccccc3c3ccccc32)cc1
title compound
المردود 99.0%
CC(OC(=O)CC12CC3CC(CC(O)(C3)C1)C2)C(F)(F)C(F)(F)S(=O)(=O)[O-].c1ccc(-[s+]2c3ccccc3c3ccccc32)cc1
5-phenyl-5H-dibenzo[b,d]thiophenium 3-hydroxyadamantane-acetoxy-1,1,2,2-tetrafluorobutane-1-sulfonate
المردود 99.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe dichloromethane layer was separated
  2. 2
    غسيلthe aqueous phase washed with dichloromethane (3×300 mL)
  3. 3
    غسيلThe combined organic layers were washed with water (4×500 mL)
  4. 4
    تركيزconcentrated in vacuo and residual water
  5. 5
    أخرىremoved via azeotrope with acetonitrile (2×350 mL)

الإجراء التجريبي

5-phenyl-5H-dibenzo[b,d]thiophenium bromide (28.0 g, 82.04 mmol) and 3-hydroxyadamantane-acetoxy-1,1,2,2-tetrafluorobutane-1-sulfonate-sodium salt (35.68 g, 83.7 mmol) were dissolved in dichloromethane (500 mL) and water (500 mL) and stirred at r.t. for 16 h. The dichloromethane layer was separated and the aqueous phase washed with dichloromethane (3×300 mL). The combined organic layers were washed with water (4×500 mL), concentrated in vacuo and residual water removed via azeotrope with acetonitrile (2×350 mL) to afford the title compound (54.00 g, 99%) as a white solid. 1H NMR (500 MHz, (CD3)2CO) δ: 8.55 (d, J=8 Hz, 2H), 8.41 (d, J=8 Hz, 2H), 8.02 (dt, J=7.5, 0.5 Hz, 2H), 7.77-7.84 (m, 5H), 7.67 (t, J=7.5 Hz, 2H), 4.31 (t, J=6.5 Hz, 2H), 3.63 (s, 10H), 2.71 (tt, J=14, 6.5 Hz, 2H), 1.52-1.80 (m, 12H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08945814B2uspto-grants-2015_02