HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918571Generated: October 31, 2026
Hydrochloric Acid → HCID 20330424, compound
https://huagongshe.com/reaction/918571
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl isothiocyanate | HCID 10966 | — |
| Reactant | 5-(Chloromethyl)-2,2,8-trimethyl-4H-(1,3)dioxino(4,5-c)pyridine | HCID 273215 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Product | HCID 20330424 | HCID 20330424 | — |
Reaction Steps
To a solution of 0.1 mole sodium ethoxide in 500 ml. of ethanol cooled to 10°-20°C. and under nitrogen is added 0.1 mole ethylisothiocyanate. The reaction mixture is stirred for 30 minutes after the addition is completed. There is then added portionwise 0.1 mole of 5-chloromethyl-2,2,8-trimethyl-4H-M-dioxino[4,5-C]-pyridine. The reaction mixture is stirred at room temperature (or refluxed 3 hours) overnight, after which time 200 ml. of 6 N hydrochloric acid is added. The reaction mixture is stirred 5 hours at room temperature, concentrated in vacuo, and the residue taken up between benzene-ether (1:1) and excess saturated sodium bicarbonate. The organic layer is separated, washed well with water, dried and concentrated to give 2-methyl-3-hydroxy-4-hydroxymethyl-5-ethoxycarbonylthiomethylpyridine and hydrochloride salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03971797 |
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| Source dataset | uspto-grants-1976_07 |
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| ORD ID | ord-a3e691b091eb4ff9817997e687db214f |
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| Source note | uspto-grants-1976_07 |
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