HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425234Generated: October 31, 2026
2-Methyltetrahydrofuran → 5-Chloro-N-((S)-2,3-dihydroxypropyl)thiophene-2-carboxamide
https://huagongshe.com/reaction/425234
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Chlorothiophene-2-carbonyl Chloride | HCID 589223 | — |
| Reactant | (S)-3-Amino-1,2-dihydroxypropane hydrochloride | HCID 53487907 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Chloro-N-((S)-2,3-dihydroxypropyl)thiophene-2-carboxamide | HCID 9991690 | — |
Reaction Steps
461 g of sodium hydrogencarbonate and 350 g of (2S)-3-aminopropane-1,2-diol hydrochloride (VII) (commercially available) are initially charged at from 13 to 15° C. in 2.1 l of water and admixed with 950 ml of 2-methyltetrahydrofuran. 535.3 g of 5-chlorothiophene-2-carbonyl chloride (approx. 93%) in 180 ml of toluene are added dropwise to this mixture with cooling at from 15 to 18° C. over a period of two hours. For workup, the phases are separated and the organic phase is admixed in several steps with a total of 1.5 l of toluene. The precipitated product is filtered off with suction, washed with ethyl acetate 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-b081fb1c16d84c258f9132468a2866a9 |
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| Source note | uspto-grants-2012_01 |
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