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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethyltetrahydrofuranHCID 7301—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Chlorothiophene-2-carbonyl ChlorideHCID 589223—
Reactant(S)-3-Amino-1,2-dihydroxypropane hydrochlorideHCID 53487907—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product5-Chloro-N-((S)-2,3-dihydroxypropyl)thiophene-2-carboxamideHCID 9991690—

Reaction Conditions

Temperature16.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106192B2
Source datasetuspto-grants-2012_01
ORD IDord-b081fb1c16d84c258f9132468a2866a9
Source noteuspto-grants-2012_01