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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863839Generated: October 29, 2026

Triethylamine → 6-Phenylhex-1-yl methylsulfonate

https://huagongshe.com/reaction/863839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant6-Phenyl-1-hexanolHCID 520110—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product6-Phenylhex-1-yl methylsulfonateHCID 13079702—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 6-phenyl-1-hexanol (3.2 g; 18 mmol) dissolved in CH2Cl2 (60 ml) is added Et3N (3.7 ml) and the solution is cooled to 0° C. Methanesulfonyl chloride (1.5 ml; 20 mmol) is added dropwise and then the reaction mixture is allowed to stir for 30 minutes at 0° C. This is then diluted with Et2O and washed with 2N HCl, NaHCO3 solution 2× and brine, dried (MgSO4) and concentrated to dryness to obtain 6-phenylhex-1-yl methylsulfonate as an oil which is used directly in Step E

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05561143
Source datasetuspto-grants-1996_10
ORD IDord-f3ef825100d1416087fda81946c3c6aa
Source noteuspto-grants-1996_10