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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798101Generated: November 1, 2026

Sodium borohydride → HCID 58292546, compound

https://huagongshe.com/reaction/1798101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantBenzyl dihydrogen borateHCID 17843933—
ReactantHCID 58292569HCID 58292569—
SolventMethanolHCID 887—
ProductHCID 58292546HCID 5829254669.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-[4-methoxy-2-methyl-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-4-oxo-butyric acid methyl ester (0.33 g, 0.87 mmol) in MeOH (3 mL) was added NaBH4 (0.073 g, 1.92 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 30 minutes, quenched with 6 N HCl and extracted with EtOAc. The organic extracts were dried and concentrated in vacuo. The residue was dissolved in CH3CN and treated with polymer-bounded benzyl boric acid (2 equiv) for 2 hours. The mixture was filtered, concentrated and purified by silica gel flash column chromatography to give 3-(1-hydroxy-6-methoxy-4-methyl-1,3-dihydro-benzo[c][1,2]oxaborol-3-yl)-propionic acid methyl ester (0.160 g, 69%). 1H NMR (400 MHz, MeOD-d4) δ 6.98 (s, 1H), 6.80 (s, 1H), 5.25 (m, 1H), 3.80 (s, 3H), 3.60 (s, 3H), 2.50-2.30 (m, 6H), 1.77 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343944B2
Source datasetuspto-grants-2013_01
ORD IDord-12bfadfe50c943edb9c57a205c81f5c6
Source noteuspto-grants-2013_01