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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | 3-(Methoxycarbonyl)-5-(N-methylmethylsulfonamido)benzoic acid | HCID 11150371 | — |
| Reactant | Acetic acid--water (1/1) | HCID 21899381 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 3-(hydroxymethyl)-5-[methyl(methylsulfonyl)amino]benzoate | HCID 57815142 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299267B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-874fb8c048114fd48054e3d11314351f |
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| Source note | uspto-grants-2012_10 |
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