Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167999Generated: October 27, 2026

Sulfuric Acid → Isopropyl 4-bromobutanoate

https://huagongshe.com/reaction/1167999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantIsopropanolHCID 3776—
Reactant4-Bromobutyric acidHCID 75809—
SolventDiethyl EtherHCID 3283—
ProductIsopropyl 4-bromobutanoateHCID 12111255—

Reaction Steps

A solution of 4-bromobutyric acid (50 g) in 2-propanol (200 mL) containing 1 mL of H2SO4 was refluxed for 3 h, then cooled to ambient temperature, diluted with ether (500 mL), washed with saturated NaHCO3 (3×300 mL), and brine (300 mL). The organic extract was dried (MgSO4), filtered and concentrated in vacuo to give isopropyl 4-bromo-butyrate (52 g) as an oil. This ester was dissolved in MeCN (380 mL). Ph3P (100 g) was added and the solution was heated at reflux for 72 h, after which TLC analysis (20% water/MeCN, C-18 RP TLC plates) showed complete reaction. The mixture was cooled and concentrated and the residue was slurried with toluene (400 mL) for 1 h. The solid was collected by filtration and was washed with toluene (100 mL) and then dried in vacuo at 50° C. to provide (3-(isopropoxycarbonyl)propyl)triphenylphosphonium bromide (100.6 g). 1H NMR (CDCl3): δ1.19-1.22 (d, 6H), 1.85-1.97 (mn, 2H), 2.85 (t, 2H), 3.95-4.10 (m, 2H), 4.89-5.03 (m, 1H), 7.65-7.94 (m, 15H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620947B2
Source datasetuspto-grants-2003_09
ORD IDord-a405a3c0dfe34b6588215a112b331d5a
Source noteuspto-grants-2003_09