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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911655Generated: October 31, 2026

Triethylamine → HCID 57656632, compound

https://huagongshe.com/reaction/911655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Cyclohexyl-hydroxy-methyl)-benzonitrileHCID 11830850—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 57656632HCID 5765663294.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Dissolve 4-(cyclohexyl-hydroxy-methyl)-benzonitrile (1 g, 4.66 mmol), and triethylamine (1.3 mL, 9.3 mmol) in dichloromethane (20 mL). Cool the mixture to 0° C., add methanesulfonyl chloride (1.49 mL, 5.34 mmol) and stir the solution for 2 h at 0° C. Add water (10 mL) and saturated aqueous NaHCO3 (10 mL). Separate the layers and extract back the aqueous phase with dichloromethane (3×20 mL). Combine the organic layers, wash with water (20 mL), dry over Na2SO4, filter and concentrate in vacuo to provide the desired intermediate as a yellow oil (1.29 g, 94%). MS (APCI) m/z: 294 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022062B2
Source datasetuspto-grants-2011_09
ORD IDord-bfd4821817a84a1a95a23f3aad553761
Source noteuspto-grants-2011_09