반응 #1929035

ord-7e3629f0375b4c91bc4c57b706ae2f1c

반응 방정식

[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
수율 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
수율 99.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The dichloromethane layer was separated
  2. 2
    세척the aqueous phase washed with dichloromethane (3×300 mL)
  3. 3
    세척The combined organic layers were washed with water (4×500 mL)
  4. 4
    농축concentrated in vacuo and residual water
  5. 5
    기타removed via azeotrope with acetonitrile (2×350 mL)

실험 절차

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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08945814B2uspto-grants-2015_02