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HRID 27396作成日:2026年10月24日

Boron trifluoride etherate → alpha-Tocopherol

https://huagongshe.com/ja/reaction/27396

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IsophytolHCID 10453—
反応物PhytolHCID 5280435—
反応物AluminumHCID 5359268—
触媒PalladiumHCID 23938—
溶媒Acetic AcidHCID 176—
溶媒Ethyl AcetateHCID 8857—
生成物alpha-TocopherolHCID 14985—

反応手順

The reaction of isophytol or phytol with TMHQ is well known. One method that has been employed with phytol is described in Japan Kokai No. 73 48,472 [Chem. Abstr. 79, 105067m (1973)]. It was discovered that a similar method could also be applied successfully in condensation of TMHQ with dehydrophytol. Essentially, 2.5 grams TMHQ and 0.1 gram aluminum powder were placed in a flask to which was added 35 mls. of ethyl acetate containing 1 ml. of boron trifluoride etherate. While stirring, 4 grams of dehydrophytol was added slowly and the mixture was refluxed for 4 hours at 80°. This gave 5.0 grams of crude dehydrotocopherol (dehydro-Vitamin E) after work-up and removal of unreacted starting materials. A portion of the dehydrotocopherol obtained (1.0 gram) was conveniently hydrogenated in 30 mls. glacial acetic acid containing 0.5 gram of 5% Pd on BaSO4. Shaking for 8 hours under 52 psig H2 pressure and ambient temperature provided 1.0 gram of crude α-tocopherol (Vitamin E). The present invention has been described with reference to the use of beta-myrcene to produce chloromyrcene (3-chloro-6-methylene-2-methylocta-1,7-diene) which is then coupled with 3,7-dimethyloctyl magnesium chloride. The invention is equally applicable to the use of alpha-myrcene, or alpha- or beta-ocimene.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04221742
出典データセットuspto-grants-1980_09
ORD IDord-2a7c2b630c264df7ba805e89635c6b78
出典メモuspto-grants-1980_09