HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425235Generated: October 30, 2026
Hydrogen Bromide → N-((S)-3-bromo-2-hydroxypropyl)-5-chlorothiophene-2-carboxamide
https://huagongshe.com/reaction/425235
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 5-Chloro-N-((S)-2,3-dihydroxypropyl)thiophene-2-carboxamide | HCID 9991690 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N-((S)-3-bromo-2-hydroxypropyl)-5-chlorothiophene-2-carboxamide | HCID 10108741 | — |
Reaction Steps
301.7 ml of a 33% solution of hydrobromic acid in acetic acid are added to a suspension of 100 g of N-((S)-2,3-dihydroxypropyl)-5-chlorothiophene-2-carboxamide (VIII) in 250 ml of glacial acetic acid at from 21 to 26° C. over a period of 30 minutes. Subsequently, 40 ml of acetic anhydride are added and the reaction mixture is stirred at from 60 to 65° C. for three hours. At 20 to 25° C., 960 ml of methanol are then added over a period of 30 minutes. The reaction mixture is stirred under reflux for 2.5 hours and then overnight at from 20 to 25° C. For workup, the solvents are distilled off under reduced pressure at approx. 95 mbar. The remaining suspension is admixed with 50 ml of 1-butanol and 350 ml of water. The precipitated product is filtered off with suction, washed with water and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106192B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-2cc01475d2b741888dc6133267712869 |
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| Source note | uspto-grants-2012_01 |
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