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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986897Generated: October 31, 2026

Pyridine → HCID 57552215, compound

https://huagongshe.com/reaction/1986897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
Reactanttert-Butyl 2-fluoro-3-hydroxypropylcarbamateHCID 6420752—
SolventDichloromethaneHCID 6344—
ProductHCID 57552215HCID 57552215—

Reaction Steps

To a suspension of NBS (20 g, 110 mmol, 3.0 equiv) in dichloromethane (250 mL) was added dropwise triphenylphosphine (28 g, 110 nmol, 3.0 equiv) in dichloromethane (100 mL). After addition was complete, the reaction mixture was stirred for 10 min and a solution of tert-butyl 2-fluoro-3-hydroxypropylcarbamate (1-8) (7.0 g, 36 mmol, 1 equiv) in dichloromethane (100 mL) followed by pyridine (3.5 g, 44 mmol, 1.2 equiv) were added. The resulting mixture was stirred at 23° C. under nitrogen for 16 h. The reaction solution was concentrated and purified by silica gel chromatography (100% hexanes to 100% ethyl acetate over 1 h, analysis by Ninhydrin stain) to yield tert-butyl 3-bromo-2-fluoropropylcarbamate (1-9) as a clear oil. 1H NMR (500 MHz, CDCl3) δ 4.89-4.68 (m, 2H), 3.55-3.40 (m, 2H), 1.45 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550477B2
Source datasetuspto-grants-2009_06
ORD IDord-d091299902bf4fbca2ddd50b77958d5e
Source noteuspto-grants-2009_06