HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057254Generated: October 26, 2026
Acetic Acid → 1-Butyl-5-ethyl-6-phenylthiouracil
https://huagongshe.com/reaction/1057254
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diphenyl disulfide | HCID 13436 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 1-Butyl-5-ethyluracil | HCID 18671032 | — |
| Product | 1-Butyl-5-ethyl-6-phenylthiouracil | HCID 54523933 | 7% |
Reaction Steps
Then, a solution of 4.4 mmol of lithium diisopropylamide in 2.8 ml of tetrahydrofuran was added dropwise to a solution of 392 mg (2.0 mmol) 1-butyl-5-ethyluracil in 9 ml of tetrahydrofuran under a nitrogen atmosphere at −70° C. and stirred for 70 minutes at −70° C. and further 5 minutes at −25° C. The mixture was cooled to −70° C. again, added with a solution of 567 mg (2.6 mmol) diphenyl disulfide in 3 ml of tetrahydrofuran, stirred for 20 minutes, added with 1 ml of acetic acid, brought to room temperature, washed with saturated aqueous solution of sodium chloride and concentrated under reduced pressure. The residue was adsorbed on a silica gel, eluted with 10% ethyl acetate/hexane and crystallized from hexane to obtain 40 mg of 1-butyl-5-ethyl-6-phenylthiouracil (Yield: 7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE037979E1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-aaafb6d740874c32a1bd59e0e0b2beee |
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| Source note | uspto-grants-2003_02 |
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