HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503085Generated: October 29, 2026
4-Methoxybenzenesulfonyl chloride → HCID 737632, compound
https://huagongshe.com/reaction/1503085
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 737632 | HCID 737632 | 134.9% |
Reaction Steps
To a solution of 4-methoxybenzenesulfonyl chloride (5.0 g, 24 mmol) and 4-methoxyaniline (3.0 g, 24 mmol) in dichloromethane (24 mL) at 0° C. was added triethylamine (3.4 mL, 24 mmol) over 10 minutes. The ice bath was removed, and the mixture was stirred for 16 hr. The mixture was diluted with dichloromethane (100 mL) and the combined solution was washed with water (50 mL) and brine (50 mL). The organic solution was dried over MgSO4, filtered, and evaporated, and the crude product was purified by silica gel chromatography (15-60% EtOAc/Hex). Product-containing fractions were pooled, evaporated, and dried under high vacuum to yield 9.5 g (79%) of the product as a tan-colored oil: 1H-NMR (DMSO-d6) δ 9.29 (s, 1H), 7.63 (d, 2H), 7.23-7.19 (m, 1H), 7.11-7.01 (m, 3H), 6.91-6.83 (m, 2H), 3.79 (s, 3H), 3.52 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212134B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-92164427766c4bd0ab69a69fe86f9cfe |
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| Source note | uspto-grants-2015_12 |
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