HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116074Generated: October 31, 2026
4-Toluenesulfonyl chloride → (+/-)-(7-Nitro-2,3-dihydro-1-benzofuran-2-yl)methyl 4-methylbenzenesulfonate
https://huagongshe.com/reaction/2116074
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (+/-)-(7-Nitro-2,3-dihydro-1-benzofuran-2-yl)methanol | HCID 11063317 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (+/-)-(7-Nitro-2,3-dihydro-1-benzofuran-2-yl)methyl 4-methylbenzenesulfonate | HCID 86599155 | 94% |
Reaction Steps
To a solution of (±)-(7-nitro-2,3-dihydro-1-benzofuran-2-yl)methanol (3.14 g, 16.09 mol) in dichloromethane (100 mL) was added diisopropylethyl amine (4.16 g, 32.18 mmol), N,N-dimethylaminopyridine (0.39 g, 3.2 mmol), and p-toluenesulfonyl chloride (4.6 g, 24.13 mmol) the reaction was allowed to stir at room temperature for 12 h. The reaction was diluted with dichloromethane (500 mL), washed with saturated aqueous sodium bicarbonate (200 mL), saturated aqueous sodium chloride (200 mL), dried (magnesium sulfate) and the solvent removed in vacuo to give a crude oil. Purification by flash column chromatography (silica, dichloromethane: hexanes 3:10) afforded 5.2 g (94%) of (±)-(7-nitro-2,3-dihydro-1-benzofuran-2-yl)methyl 4-methylbenzenesulfonate as off-white solid. mp 129-131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07435837B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-423c347516624bbfa48f9d5e2c0b7b91 |
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| Source note | uspto-grants-2008_10 |
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