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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611101Generated: November 1, 2026

Phenylmethanesulfonyl chloride → HCID 9874688, compound

https://huagongshe.com/reaction/1611101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylmethanesulfonyl chlorideHCID 74740—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 16116212HCID 16116212—
SolventDichloromethaneHCID 6344—
ProductHCID 9874688HCID 987468886%

Reaction Steps

To methyl 4-{2-[2-(2-aminoethyl)-1-benzhydryl-5-chloro-1H-indol-3-yl]ethoxy}benzoate (1.0 equiv) and sat. NaHCO3 (0.14 M) in CH2Cl2 (0.07 M) was added α-toluenesulfonyl chloride (1.0 equiv). After 1 h the mixture was poured into saturated sodium bicarbonate and extracted with CH2Cl2. The combined organic phase was washed with brine, dried over sodium sulfate and purified by column chromatography (gradient elution using 20% EtOAc-hexanes→50% EtOAc-hexanes) to afford 86% of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984735B2
Source datasetuspto-grants-2006_01
ORD IDord-1ab38e736d0b48f3ad7d14aaf4e71ec7
Source noteuspto-grants-2006_01