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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338401Generated: October 29, 2026

Formaldehyde → 3-(4-Bromophenyl)-1-methylpyrrolidine

https://huagongshe.com/reaction/338401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantTriethylamineHCID 8471—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-(4-Bromophenyl)pyrrolidine hydrochlorideHCID 53407708—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
Product3-(4-Bromophenyl)-1-methylpyrrolidineHCID 59428427135.3%

Reaction Steps

To a mixture of 3-(4-bromophenyl)pyrrolidine hydrochloride (200 mg, 0.76 mmol) in methanol (6 mL) was added triethylamine (77 mg, 0.76 mmol) and several drops of acetic acid. The reaction mixture was stirred at room temperature for 5 min and treated with aqueous formaldehyde (37%, 0.2 mL) and sodium triacetoxyborohydride (322 mg, 1.52 mmol). The reaction mixture was stirred for 18 h at room temperature. The methanol was evaporated in vacuo and the residue was partitioned between water and EtOAc. The phases were separated and the aqueous phase was back-extracted with EtOAc. The combined organic phases were washed with brine, dried over Na2SO4, and concentrated in vacuo to give 3-(4-bromophenyl)-1-methylpyrrolidine (0.247 g) as a solid, which was used in the next step without further purification. MS (ES+) 239.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-5f15b8b6d26348d09f025311a0379085
Source noteuspto-grants-2014_11