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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561333Generated: October 30, 2026

P-Anisidine → HCID 59718039, compound

https://huagongshe.com/reaction/561333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantTriethylamineHCID 8471—
ReactantHCID 59717988HCID 59717988—
SolventDichloromethaneHCID 6344—
ProductHCID 59718039HCID 59718039—

Reaction Steps

To a solution of 5-benzoylamino-naphthalene-1-sulfonyl chloride 44 (0.1 g, 0.29 mmol) in dichloromethane (0.5 mL) was added triethylamine (0.06 ml, 0.43 mmol) and p-anisidine (0.05 g, 0.3 mmol). The resultant solution stirred at room temperature for 3 hours. The reaction mixture was quenched with water and the compound extracted into ethyl acetate. The organic extracts were washed with brine, dried over MgSO4, filtered and concentrated to provide the crude product as a yellow oil. 1H NMR (300 MHz, DMSO) δ 8.65 (d, 1H), 8.19 (d, 1H), 8.06 (m, 3H), 7.70 (m, 2H), 7.54 (m, 2H), 6.84 (d, 2H), 6.69 (d, 2H), 3.56 (s, 3H); LC/MS (M+H)+ m/z 433.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063222B2
Source datasetuspto-grants-2011_11
ORD IDord-0c9f3839e8574c5ea61e4357454e6562
Source noteuspto-grants-2011_11