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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217783Generated: October 26, 2026

Boron trifluoride etherate → 3-(4-Bromophenyl)propan-1-ol

https://huagongshe.com/reaction/217783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantTetrahydrofuranHCID 8028—
Reactant3-(2-Bromophenyl)propionic acidHCID 316010—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
Solventtert-Butyl methyl etherHCID 15413—
Product3-(4-Bromophenyl)propan-1-olHCID 10560614—

Reaction Conditions

Temperature25 °C

Reaction Steps

Sodium borohydride (119.12 g) and THF (5 L) were charged into reactor 1 and temperature adjusted to −20° C. 3-(bromophenyl)propionic acid (1 kg) was charged into reactor 2 with THF (3 L) and stirred at 25° C. until all the solids dissolved. This solution in reactor 2 was transferred to reactor 1 maintaining reactor 1 contents at <0° C. BF3.Et2O (991.4 g) was slowly added into reactor 1 maintaining reactor 1 contents at −20 to −10° C. After addition, the mixture was stirred at −20 to −10° C. for 1 h. The reaction is analysed for completion (3-(bromophenyl)propionic acid <2.5%). Water (2 L) was slowly added into reactor 1 to quench the reaction. (gas evolution). MTBE (5 L) was charged into reactor 1 and phases separation was carried out. The upper layer was collected and lower layer was washed with MTBE (5 L). The upper layer was collected and combined with the layer from the previous step. Adjusted pH value of the organic layer to 8-9 by adding 1N NaOH solution. The organic layer was washed with saturated NaCl solution (2 L) and the upper layer was collected. The organic layer was evaporated down to a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198285B2
Source datasetuspto-grants-2012_06
ORD IDord-34040895c7734d0f8dcdc8093bf0d886
Source noteuspto-grants-2012_06