참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Phenol | HCID 996 | — |
| 반응물 | Phosgene | HCID 6371 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Phosgene phenol | HCID 86748739 | — |
| 촉매 | Triphenyl phosphite | HCID 7540 | — |
| 생성물 | Phenyl chloroformate | HCID 15891 | 96.3% |
반응 단계
A four-necked flask equipped with a gas inlet, a dry ice condenser, a mechanical stirrer, a thermocouple and a sampling port is charged with phenol (Aldrich, 287.5 g, 2.907 mol) and triphenyl phosphite (10.12 g, 32.61 mmol). The temperature is raised to 140° C. and phosgene (274 g, 2.77 mol) is added over a 465 minute period. Phosgene/phenol molar ratio is 0.95. A recirculating aqueous sodium hydroxide scrubber is used to neutralize the coproduct hydrochloric acid and to destroy traces of phosgene which are not condensed in the condenser. After the phosgene addition is stopped, a nitrogen stream is used to purge residual phosgene and the reactor is cooled to ambient temperature. The colorless crude product is isolated by vacuum distillation to give phenyl chloroformate (417.84 g, bp 73°-77° C. at 14 mm Hg) containing 6.6 percent by weight residual phenol. Selectivity to phenyl chloroformate is 95 mole percent based on phenol, 90 mole percent based on phosgene.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05424473 |
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| 출처 데이터셋 | uspto-grants-1995_06 |
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| ORD ID | ord-a0df9aa2b5d94cfb8738aba40dd8ebff |
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| 출처 메모 | uspto-grants-1995_06 |
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