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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424942Generated: October 25, 2026

Sodium borohydride → 5-Bromo-2-benzothiazoleethanol

https://huagongshe.com/reaction/424942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 2-(5-bromobenzo[D]thiazol-2-YL)acetateHCID 21041508—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-2-benzothiazoleethanolHCID 21980060—

Reaction Steps

(5-Bromo-benzothiazol-2-yl)-acetic acid ethyl ester (1.25 g, 4.2 mmol) was dissolved in THF (20 mL) and EtOH (5 mL) under N2. Then 0.24 g of NaBH4 was dissolved in EtOH (3 mL) and added to the above solution. The reaction mixture was stirred at room temperature for 2 hours. After the completion the mixture was quenched with water and extracted with CH2Cl2. The aqueous layer was extracted again with more CH2Cl2. The combined methylene chloride layer was dried over anhydrous MgSO4 and filtered. Removal of solvent gave crude product with a yield of 1.11 g. The crude product was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106088B2
Source datasetuspto-grants-2012_01
ORD IDord-ff17e187b6fb4ebc8394b709caf4a69d
Source noteuspto-grants-2012_01