참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | (+-)-4-Hydroxymandelic acid | HCID 328 | — |
| 반응물 | Ethylene Oxide | HCID 6354 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 촉매 | Sodium Hydroxide | HCID 14798 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-(2-Hydroxyethoxy)mandelic acid | HCID 19930444 | 89.3% |
반응 단계
1040.8 g (5.00 mol) of 4-hydroxymandelic acid, sodium salt monohydrate, 10.0 g (0.25 mol) of sodium hydroxide and 1000 ml of water are placed in an autoclave of 6.3 liter capacity. The autoclave is flushed with nitrogen and 330.4 g (7.50 mol) of ethylene oxide are then injected. The contents are slowly heated to 95° C. over a period of 2 hours with stirring and stirred at this temperature for another 2 hours. The still hot reaction mixture is poured into another vessel, acidified at 95° C. with 540 ml (about 5.5 mol) of 32% hydrochloric acid and crystallized by slow cooling to about +10° C. The precipitated product is filtered with 1000 ml of cold water and dried to give 948 g (89%) of 4-(2-hydroxyethoxy)mandelic acid, m.p. 162°-164° C. (compound (201), Table 2).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05428162 |
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| 출처 데이터셋 | uspto-grants-1995_06 |
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| ORD ID | ord-c67edfe10f0c42c1817b3ec1f6f83abd |
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| 출처 메모 | uspto-grants-1995_06 |
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