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HRID 217783作成日:2026年10月26日

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

https://huagongshe.com/reaction/217783

反応式

関与物質

役割名称HCID仕込み量
反応物Boron trifluoride etherateHCID 8000—
反応物TetrahydrofuranHCID 8028—
反応物3-(2-Bromophenyl)propionic acidHCID 316010—
反応物Sodium borohydrideHCID 4311764—
溶媒WaterHCID 962—
溶媒tert-Butyl methyl etherHCID 15413—
生成物3-(4-Bromophenyl)propan-1-olHCID 10560614—

反応条件

温度25 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198285B2
出典データセットuspto-grants-2012_06
ORD IDord-34040895c7734d0f8dcdc8093bf0d886
出典メモuspto-grants-2012_06