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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071055Generated: October 31, 2026

Borane;tetrahydrofuran → Methyl 3-(hydroxymethyl)-5-[methyl(methylsulfonyl)amino]benzoate

https://huagongshe.com/reaction/2071055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant3-(Methoxycarbonyl)-5-(N-methylmethylsulfonamido)benzoic acidHCID 11150371—
ReactantAcetic acid--water (1/1)HCID 21899381—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-(hydroxymethyl)-5-[methyl(methylsulfonyl)amino]benzoateHCID 5781514286%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a stirring solution of 234 mg of 3-(methoxycarbonyl)-5-(N-methylmethylsulfonamido)benzoic acid in 10 mL of THF at r.t. was added 1.2 mL of BH3.THF (1.0 M in THF). After the solution was stirred at 75° C. for 3 h, 3 mL of acetic acid:H2O (1:1) was added and stirring was continued until bubbling ceased. Saturated NaHCO3 solution was added to a pH=7, and the solution was concentrated. Water was added, and the aqueous layer was extracted with EtOAc (2×). The combined extracts were washed with water and brine, dried over Na2SO4, filtered, and concentrated. Purification by flash silica gel chromatography (1.5% MeOH/CHCl3) provided 191 mg of methyl 3-(hydroxymethyl)-5-(N-methylmethylsulfonamido)benzoate as a pale yellow oil in 86% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299267B2
Source datasetuspto-grants-2012_10
ORD IDord-874fb8c048114fd48054e3d11314351f
Source noteuspto-grants-2012_10