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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459598Generated: November 2, 2026

Sodium Sulfate → 6-Methoxy-2-phenyl-5-hydroxymethylbenzothiazole

https://huagongshe.com/reaction/1459598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfateHCID 24436—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethyl-6-methoxy-2-phenyl-5-benzothiazolcarboxylateHCID 22620051—
SolventTetrahydrofuranHCID 8028—
Product6-Methoxy-2-phenyl-5-hydroxymethylbenzothiazoleHCID 22620081—

Reaction Conditions

Temperature0 °C

Reaction Steps

A 1 liter round bottom flask was charged with 12.88 grams (45.2 mmol) of methyl-6-methoxy-2-phenyl-5-benzothiazolecarboxylate (as part of a mixture of regioisomeric carboxylates) in 600 mL of dry tetrahydrofuran (THF). This solution was cooled to 0° C. and treated with 67.8 mL (67.8 mmol) of a 1.0M solution of lithium aluminum hydride in THF. The dark reaction mixture was stirred for 5 hours under nitrogen. The reaction was worked up by the careful dropwise addition of a saturated aqueous solution of sodium sulfate until a granular precipitate formed. The suspension was filtered and evaporated. The residue was dissolved in ethyl acetate and washed with water and saturated brine solution. The organic phase was dried over sodium sulfate and evaporated. This product was used directly in the next step. (10.94 grams crude yield)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854262
Source datasetuspto-grants-1998_12
ORD IDord-8244240943094a13b1ffdf8bae1c696a
Source noteuspto-grants-1998_12