HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199575Generated: October 29, 2026
Acetic Acid → Methyl 2-[5-bromo-2-(4-methanesulfonylphenyl)thiophen-3-yl]acetate
https://huagongshe.com/reaction/2199575
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 2-[2-(4-methanesulfonylphenyl)thiophen-3-yl]acetate | HCID 71230756 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Methyl 2-[5-bromo-2-(4-methanesulfonylphenyl)thiophen-3-yl]acetate | HCID 71230633 | — |
Reaction Steps
NBS (209 mg, 1.18 mmol) was added in small portions to a stirred solution of Intermediate Y (365 mg, 1.18 mmol) in a mixture of MeOH (10 ml) and chloroform (5 ml) at 0° C. AcOH (0.250 ml) was added and the reaction was stirred at 0° C. for 1 hour then at r.t. for 3 hours. More NBS (35 mg, 0.20 mmol) was added at 0° C. and the reaction was stirred at r.t. over night. A new reaction was also started. NBS (342 mg, 1.92 mmol) was added in small portions to a stirred solution of Intermediate Y (519 mg, 1.67 mmol) in a mixture of MeOH (15 ml) and chloroform (7 ml) at 0° C. AcOH (0.50 ml) was added and the reaction was stirred at r.t. over night.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359311B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-a153574c1492456483680e7e878b5fcc |
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| Source note | uspto-grants-2016_06 |
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