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HRID 1701236作成日:2026年10月26日

Phosphoric Acid → (S)-(+)tert. Butyl 3-tert. butoxy-2-methylpropionate

https://huagongshe.com/reaction/1701236

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphoric AcidHCID 1004—
反応物DichloromethaneHCID 6344—
反応物Boron trifluoride etherateHCID 8000—
反応物IsobutyleneHCID 8255—
反応物Sodium BicarbonateHCID 516892—
反応物Acetone cardiceHCID 18522661—
溶媒WaterHCID 962—
生成物(S)-(+)tert. Butyl 3-tert. butoxy-2-methylpropionateHCID 12923317—

反応条件

温度-72 °C

反応手順

A solution of 8.7 g. of S-(+)-β-hydroxyisobutyric acid in 140 ml. of CH2Cl2 was stirred and cooled to -72° C. (dry ice-acetone bath) whereupon 70 ml. of liquid isobutylene was added rapidly. To the resulting mixture was added with stirring at -72° C., a solution of 1.6 ml. of phosphoric acid (prepared by dissolving 5 g. of phosphorus pentoxide in 11 ml. of 85% by weight phosphoric acid) in 10 ml. of CH2Cl2, dropwise followed by 3.5 ml. of boron trifluoride etherate also dropwise. The resulting mixture was stirred at -72° C. for 2 hours and at 0°-5° C. (ice bath) for 20 hours then treated with 300 g. of ice-water followed by a solution of 19 g. of NaHCO3 in 200 ml. of water. The CH2Cl2 layer was removed and the aqueous layer was extracted twice with CH2Cl2. The combined organic extracts were washed twice with brine then dried (MgSO4), filtered and concentrated in vacuo giving 23.3 g. of crude product as a yellow oil. This material was chromatographed on 200 g. of silica gel. Elution with 19:1 parts by volume and 9:1 parts by volume hexane-ether gave the desired product which was distilled yielding 12.7 g. (79%) of the ether ester (S)-(+)-tert. butyl 3-tert. butoxy-2-methylpropionate as a colorless liquid, b.p. 99° C. (22 mm Hg.); [α]25D+19.52° (c 4.25, CH3OH).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04191842
出典データセットuspto-grants-1980_03
ORD IDord-d090a6e045324249bb1bd1bce9816cad
出典メモuspto-grants-1980_03