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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503085Generated: October 29, 2026

4-Methoxybenzenesulfonyl chloride → HCID 737632, compound

https://huagongshe.com/reaction/1503085

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantP-AnisidineHCID 7732—
ReactantTriethylamineHCID 8471—
SolventDichloromethaneHCID 6344—
ProductHCID 737632HCID 737632134.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212134B2
Source datasetuspto-grants-2015_12
ORD IDord-92164427766c4bd0ab69a69fe86f9cfe
Source noteuspto-grants-2015_12