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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103317Generated: November 2, 2026

Triethylamine → HCID 68998458, compound

https://huagongshe.com/reaction/2103317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 3-bromopropanoateHCID 76934—
ReactantHCID 24883357HCID 24883357—
SolventDichloromethaneHCID 6344—
ProductHCID 68998458HCID 6899845868%

Reaction Steps

To a solution of 4-(4-Phenoxy-phenoxy)-piperidine (152 mg, 0.5 mmol) in anhydrous CH2Cl2 (0.5 mL) was added methyl-3-bromopropionate (99 mg, 0.55 mmol) in CH2Cl2 (0.5 mL) and triethylamine (101 mg, 1.0 mmol). The resulting mixture was purged with nitrogen and stirred at if for 48 h. CH2Cl2 was removed in vacuo and crude mixture was partioned between EtOAc and water. EtOAc layer was removed, washed with brine, dried over anhydrous MgSO4 and concentrated. The crude mixture was purified by silica gel flash chromatography (40-70% EtOAc/Hexane) to obtain the product as yellow oil (125 mg, 68%): 1H NMR (400 MHz, DMSO-d6); δ 1.54-1.69 (m, 4H), 1.89-1.92 (m, 2H), 2.14-2.18 (m, 2H), 2.26-2.33 (m, 4H), 2.64-2.67 (m, 2H), 3.58 (s, 3H), 4.27-4.31 (m, 1H), 6.91-6.96 (m, 6H), 7.04-7.08 (m, 1H), 7.32-7.36 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576102B2
Source datasetuspto-grants-2009_08
ORD IDord-e549668bbc9444d2a07015e8d8c5527b
Source noteuspto-grants-2009_08