HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 993265Generated: October 29, 2026
Lithium borohydride → HCID 22145918, compound
https://huagongshe.com/reaction/993265
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 22145785 | HCID 22145785 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 22145918 | HCID 22145918 | 79.5% |
Reaction Steps
A stirred solution of N-(2,6-dichloro-4-ethoxycarbonylphenyl)-3-cyclopentyloxy-4-methoxybenzamide (6.1 g) 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06472412B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-4967412fdff34006b42b3a65c79b2b48 |
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| Source note | uspto-grants-2002_10 |
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