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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383477Generated: October 31, 2026

Lithium borohydride → HCID 22145918, compound

https://huagongshe.com/reaction/1383477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 22145785HCID 22145785—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 22145918HCID 22145918—

Reaction Steps

A stirred solution of N-(2,6-dichloro-4-ethoxycarbonylphenyl)-3-cyclopentyloxy-4-methoxybenzamide (6.1 g; that is prepared as described in Example 8) in dry tetrahydrofuran (80 mL) at room temperature under argon is treated dropwise with a solution of lithium borohydride in tetrahydrofuran (115 mL; 2 M). The mixture is stirred overnight and then it is treated portionwise with saturated brine (200 mL) and stirred for 30 minutes. The organic layer is then washed with water, dried over magnesium sulfate and evaporated. The resulting residue is subjected to flash chromatography on silica gel, to give N-(2,6-dichloro-4-hydroxymethylphenyl)-3-cyclopentyloxy-4-methoxybenzamide (4.4 g), m.p. 174-176° C. [Elemental analysis: C,57.1; H,5.4; N,2.9%; calculated C20H21O4NCl2:0.5H2O: C,57.3; H,5.3; N,3.3%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255326B1
Source datasetuspto-grants-2001_07
ORD IDord-9d037aa9eedd4a74a573522fd695a52c
Source noteuspto-grants-2001_07