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HRID 2072819作成日:2026年10月27日

Phosphoric Acid → Phosphoric acid, monoisopropanolate salt

https://huagongshe.com/reaction/2072819

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TetramethylureaHCID 12437—
反応物1-Chloroethyl pivalateHCID 3016174—
反応物3-Hydroxy-N-methyl-L-tyrosineHCID 23620856—
溶媒TolueneHCID 1140—
生成物Phosphoric acid, monoisopropanolate saltHCID 131715176—

反応条件

温度70 °C

反応手順

In an operation carried out in a manner similar to that described in Example 1, 42.3 grams (0.2 mole) of methyldopa, 40.3 milliliters (0.24 mole) of 1-chloroethyl pivalate, 14 grams of 4A molecular sieve pellets (1/16") and 85 milliliters of tetramethylurea are mixed together and heated in an atmosphere of nitrogen to 70° C. and maintained at this temperature for about 30 hours. During this time, the methyldopa dissolves with the formation of (R,S)-1-pivaloyloxyethyl ester product. Thereafter, the reaction mixture is cooled to 25° C. and diluted with 380 milliliters of toluene. The mixture is then washed with three 500 milliliter portions of saturated sodium bicarbonate solution and filtered to clarify the solution. To this solution is added 300 milliliters of isopropanol followed by 16.6 grams (0.14 mole) of 85 percent phosphoric acid and 0.100 gram of methyldopa (R,S)-POE ester phosphoric acid monoisopropanolate seed whereupon the product crystallizes. The crystal-containing slurry is aged for 16 hours at 20°-25° C., then filtered and washed with two 75 milliliter portions of isopropanol and dried in vacuo to obtain (R,S)-1-pivaloyloxyethyl (S)-3-(3,4-dihydroxyphenyl)-2-methylalaninate, phosphoric acid, monoisopropanolate salt.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04914222
出典データセットuspto-grants-1990_04
ORD IDord-2e7e396d3bf4467b88790bf8e9fee352
出典メモuspto-grants-1990_04