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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840607Generated: October 29, 2026

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

https://huagongshe.com/reaction/840607

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 1.0 M 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 numberUS06369074B1
Source datasetuspto-grants-2002_04
ORD IDord-66b81aee6c1b4a1b8ca0ec7abacd9417
Source noteuspto-grants-2002_04