HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729298Generated: November 2, 2026
4-Aminobenzyl alcohol → HCID 11574576, compound
https://huagongshe.com/reaction/729298
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminobenzyl alcohol | HCID 69331 | — |
| Reactant | 2-Butyl-4-chloro-5-phenylisothiazol-3(2H)-one 1,1-dioxide | HCID 67242623 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11574576 | HCID 11574576 | 4.7% |
Reaction Steps
2-Butyl-4-chloro-5-phenylisothiazol-3(2H)-one 1,1-dioxide (110 mg, 0.331 mmol) was dissolved in dry DMF (0.5 mL) under nitrogen atmosphere. (4-Aminophenyl)methanol (122 mg, 0.991 mmol) was added and the reaction mixture was heated in a microwave reactor for 25 mins at 140° C. The crude product was purified by preparative HPLC affording the title compound (6 mg, 4.7%). 1H NMR (500 MHz, CD3CN): δ 1.00 (t, 3H), 1.43-1.52 (m, 2H), 1.78-1.85 (m, 2H), 3.03 (t, 1H), 3.75 (t, 2H), 4.40 (d, 2H), 6.77 (d, 2H), 6.97 (d, 2H), 7.13-7.19 (m, 4H), 7.24-7.28 (m, 1H), 7.76 (bs, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582629B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-d23091d828e04d1bb5524b62a8abd441 |
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| Source note | uspto-grants-2009_09 |
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