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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157101Generated: November 2, 2026

Triethylamine → HCID 86616918, compound

https://huagongshe.com/reaction/1157101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(S)-1,4-pentanediolHCID 7271800—
SolventEthyl AcetateHCID 8857—
ProductHCID 86616918HCID 8661691898%

Reaction Conditions

Temperature5 °C

Reaction Steps

A solution containing 2.5 g (24 mmol) of (S)-1,4-pentanediol produced in Example 3, 7.3 g (72 mmol) of triethylamine, and 30 mL of ethyl acetate was cooled to 5° C. Subsequently, 6.6 g (58 mmol) of methanesulfonyl chloride was added to the solution, and the solution was stirred for one hour. The solution was washed by adding 15 mL of a saturated aqueous solution of sodium hydrogencarbonate. The organic layer was further washed with 15 mL of water, and was dried over anhydrous magnesium sulfate. The solvent was then distilled off under a reduced pressure. Thus, (S)-1,4-bis(methanesulfonyloxy)pentane was obtained as a light yellow oily substance (6.1 g, yield; 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807426B2
Source datasetuspto-grants-2010_10
ORD IDord-6fef562ccffe4b36acae5c717b9bc0ab
Source noteuspto-grants-2010_10