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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408500Generated: October 31, 2026

Sodium borohydride → HCID 11774705, compound

https://huagongshe.com/reaction/408500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58609757HCID 58609757—
SolventMethanolHCID 887—
ProductHCID 11774705HCID 1177470565.2%

Reaction Steps

1-Benzo[1,3]dioxol-5-yl-cyclopropanecarboxylic acid [5-(2-chloro-benzoyl)-thiazol-2-yl]-amide (1.0 g, 2.3 mmol) was suspended in 150 mL of anhydrous methanol. Sodium borohydride (1.3 g, 35 mmol) was slowly added and the resulting pale yellow solution was allowed to stir for 1 hour at room temperature. The crude product was evaporated to dryness and then dissolved in a minimum of ethyl acetate. The organic was washed three times with an equal volume of 1N hydrochloric acid, saturated aqueous sodium bicarbonate, and saturated aqueous sodium chloride. The organic layer was then dried over sodium sulfate, filtered, and evaporated to dryness to yield the product as a beige solid (0.64 g, 1.5 mmol, 63%) ESI-MS m/z calc. 428.1. found; 429.5 (M+1)+ Retention time 3.17 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759335B2
Source datasetuspto-grants-2014_06
ORD IDord-109530e8ba7940dc92d4b065659ddce4
Source noteuspto-grants-2014_06