HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731750Generated: November 1, 2026
Sodium Bicarbonate → HCID 13505217, compound
https://huagongshe.com/reaction/1731750
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | But-1-ene-1,1-diol | HCID 12429743 | — |
| Reactant | HCID 13371549 | HCID 13371549 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 13505217 | HCID 13505217 | 27.2% |
Reaction Steps
Under argon, 720 mg (2 mmol) of 6-iodo-4-methyl-β-carboline-3-carboxylic acid ethyl ester is heated in a pressure vessel with 202 mg (2.4 mmol) of sodium bicarbonate, 75 mg (0.42 mmol) of palladium dichloride, and 705 mg (8 mmol) of butenediol in 10 ml of N-methylpyrrolidone for 2 hours to 150° C. After filtration and concentration, the mixture is distributed in ethyl acetate/water. The aqueous phase is extracted twice with ethyl acetate, the combined organic phases are dried, filtered, and concentrated. The residue is chromatographed over silica gel with toluene:ethanol=80:40 as the eluent. Recrystallization of the corresponding fractions from ethyl acetate/diisopropyl ether yields 185 mg (26% of theory) of 6-(2-hydroxytetrahydrofuran-4-yl)-4-methyl-β-carboline-3-carboxylic acid ethyl ester, mp 177°-180° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04623649 |
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| Source dataset | uspto-grants-1986_11 |
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| ORD ID | ord-9cc3ddac91e2460aac35edfb49ef9e2c |
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| Source note | uspto-grants-1986_11 |
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