HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841853Generated: November 2, 2026
Water → 5-phenyl-5H-dibenzo[b,d]thiophenium 3-hydroxyadamantane-acetoxy-1,1,2,2-tetrafluorobutane-1-sulfonate
https://huagongshe.com/reaction/1841853
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 5-Phenyl-5H-dibenzo[b,d]thiophen-5-ium Bromide | HCID 86712456 | — |
| Reactant | 3-Hydroxyadamantane acetoxy-1,1,2,2-tetrafluorobutane-1-sulfonate sodium | HCID 131732410 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-phenyl-5H-dibenzo[b,d]thiophenium 3-hydroxyadamantane-acetoxy-1,1,2,2-tetrafluorobutane-1-sulfonate | HCID 131732409 | 99% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08945814B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-7e3629f0375b4c91bc4c57b706ae2f1c |
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| Source note | uspto-grants-2015_02 |
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