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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619734Generated: November 1, 2026

Dichloromethane → HCID 59830380, compound

https://huagongshe.com/reaction/1619734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantHCID 11159600HCID 11159600—
ReactantHCID 86624330HCID 86624330—
SolventWaterHCID 962—
ProductHCID 59830380HCID 59830380—

Reaction Steps

Compound C (3.9 g, 25.2 mmol, dissolved in abs. DCM (25 ml)) was added dropwise to a solution of 1-benzyl-3-methylenepyrrolidine (P) (2.18 g, 12.6 mmol) in abs. DCM (25 ml) at 0° C. within 10 min. A solution of triethylamine (14 ml, 10.2 g, 100.1 mmol) in abs. DCM (25 ml) was added to this mixture at 0° C. within 10 min. As the reaction was highly exothermic, cooling was carried out in an ice/sodium chloride mixture. The reaction mixture was stirred for 16 h at RT. For working up the mixture, DCM (50 ml) and water (70 ml) were added. The phases were separated. The aqueous solution was extracted with DCM (2×20 ml). The combined organic phases were washed successively with water (50 ml) and sat. NaCl solution (50 ml) and then dried and concentrated (5.3 g, yellow oil). The residue was purified by column chromatography [silica gel 60 (500 g); EtOAc/cyclohexane 1:2 (3 l)]. The desired compound Q was obtained as a solid in a yield of (2.4 g, 65%) having a melting point of 31-40° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772307B2
Source datasetuspto-grants-2014_07
ORD IDord-c8673d2ac88d4c7682f49ca57bcbaf1a
Source noteuspto-grants-2014_07