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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478962Generated: November 2, 2026

Triethylamine → HCID 57500205, compound

https://huagongshe.com/reaction/1478962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantBenzyl 5-hydroxypentanoateHCID 19788674—
SolventDichloromethaneHCID 6344—
ProductHCID 57500205HCID 5750020553.3%

Reaction Steps

To a solution of benzyl 5-hydroxypentanoate (2.01 g, 9.65 mmol) in anhydrous dichloromethane (30 mL) under nitrogen at −15° C. was added triethylamine (2.7 mL, 19.3 mmol) followed by a solution of methanesulfonyl chloride (1.5 mL, 19.3 mmol) dropwise over 20 minutes. The reaction was stirred at room temperature overnight and then diluted to 75 mL using dichloromethane. The organic layer was washed three times with saturated NaHCO3 and the combined aqueous layers backextracted with dichloromethane. The combined organic phases were dried over MgSO4, filtered, and concentrated. The resulting dark orange oil was purified by column chromatography (column 5″L×1″W; eluted with a gradient of 100% hexanes→10%→20%→25% diethyl ether in hexanes) to afford the product as a pale yellow oil (1.39 g, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09404127B2
Source datasetuspto-grants-2016_08
ORD IDord-4da1cf4030e6453ead0c580c43233856
Source noteuspto-grants-2016_08