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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223547Generated: October 27, 2026

Tetrahydrofuran → 2-Methyl-3-hydroxy-4-mercaptomethyl-5-vinylpyridine

https://huagongshe.com/reaction/223547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantEther tetrahydrofuranHCID 21868444—
ReactantHCID 178437128HCID 178437128—
Product2-Methyl-3-hydroxy-4-mercaptomethyl-5-vinylpyridineHCID 13066946—

Reaction Steps

The isothioureido compound from Example 25, Step A, (0.1 mole) in 200 ml. of tetrahydrofuran:ether (3:1 v/v) is added to excess lithium aluminum hydride under ether and nitrogen at 0° C. over 30 minutes. After stirring one hour at room temperature, it is poured into a mixture of tetrahydrofuran and saturated ammonium chloride solution. The water layer is separated and extracted with 2×400 ml. of tetrahydrofuran. The combined tetrahydrofuran solutions are dried and evaporated to dryness to give 2-methyl-3-hydroxy-4-mercaptomethyl-5-vinylpyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04355034
Source datasetuspto-grants-1982_10
ORD IDord-ab808fc495a84753b32b1df2c9a5c120
Source noteuspto-grants-1982_10