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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1701236생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1701236

반응식

참여 물질

역할이름HCID투입량
반응물Phosphoric AcidHCID 1004—
반응물DichloromethaneHCID 6344—
반응물Boron trifluoride etherateHCID 8000—
반응물IsobutyleneHCID 8255—
반응물Sodium BicarbonateHCID 516892—
반응물Acetone cardiceHCID 18522661—
용매WaterHCID 962—
생성물(S)-(+)tert. Butyl 3-tert. butoxy-2-methylpropionateHCID 12923317—

반응 조건

온도-72 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04191842
출처 데이터셋uspto-grants-1980_03
ORD IDord-d090a6e045324249bb1bd1bce9816cad
출처 메모uspto-grants-1980_03