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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375089Generated: October 29, 2026

Phosphorus tribromide → HCID 15291211, compound

https://huagongshe.com/reaction/375089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus tribromideHCID 24614—
ReactantN-[4-(Hydroxymethyl)phenyl]-N-methylacetamideHCID 54439979—
SolventDichloromethaneHCID 6344—
ProductHCID 15291211HCID 1529121181%

Reaction Steps

To a solution of 4-(N-acetyl-N-methylamino)benzyl alcohol (543.0 mg, 3.0 mmol), prepared as in step 2, dissolved in dry CH2Cl2 (11.5 mL) was added dropwise 1M PBr3 in CH2Cl2 (3.6 mL, 3.6 mmol) at 0° C. The reaction was stirred at ambient temperature until TLC indicated complete reaction (~5 hours). The resulting solution was partitioned between ethyl acetate and brine. The combined organic layers were decolorized with charcoal, dried (MgSO4), filtered through celite and concentrated in vacuo. Purification by flash chromatography on silica gel (40% ethyl acetate/hexane) provided 4-(N-acetyl-N-methylamino)benzyl bromide as a colorless solid (595 mg, 81.0%). 1H NMR (300 MHz, CDCl3) δ7.46 (2H, d, J=8.5 Hz), 7.18 (2H, d, J=8.5 Hz), 4.50 (2H, s), 3.27 (3H, s), 1.88 (3H, br s). MS m/e 242 (M+H)+, 259/261 (M+NH4)+. Analysis calc'd for C10H12NOBr: C, 49.61; H, 5.00; N, 5.79. Found: C, 49.35; H, 4.97; N, 5.65.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484786
Source datasetuspto-grants-1996_01
ORD IDord-0496722f836b439792c5716c61f918f6
Source noteuspto-grants-1996_01