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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602464Generated: October 30, 2026

Triethylamine → HCID 86624148, compound

https://huagongshe.com/reaction/602464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 67270690HCID 67270690—
SolventDichloromethaneHCID 6344—
ProductHCID 86624148HCID 86624148—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of tert-butyl trans-2-(3-ethoxy-3-oxopropyl)-5-hydroxypiperidine-1-carboxylate (625 mg, 2.07 mmol, step 3 of Example 5) and triethylamine (252 mg, 2.49 mmol) in dichloromethane (9.0 mL) was added methanesulfonyl chloride (285 g, 2.49 mmol) at 0° C. The resulting mixture was stirred at 0° C. for 2 h and then stirred at room temperature for 20 h. The mixture was quenched with water (30 mL), extracted with dichloromethane (30 mL×4). The combined organic layer was dried over magnesium sulfate and concentrated under reduced pressure to give 790 mg (quant.) of the title compound as a yellow oil. The resulting residue was used for the next reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906532B2
Source datasetuspto-grants-2011_03
ORD IDord-4ec07f9ab41a4e68951e5a0983f9431e
Source noteuspto-grants-2011_03