참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Ethylenediamine | HCID 3301 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 3-Dodecynoic acid, 11-hydroxy- | HCID 10899930 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 촉매 | Nickel Acetate | HCID 9756 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Sodium Hydroxide | HCID 14798 | — |
| 용매 | Sodium chloride; water | HCID 57417360 | — |
| 생성물 | 11-hydroxy-3Z-dodecenoic acid | HCID 86740560 | 96.4% |
반응 단계
To a vigorously stirred mixture of nickel acetate (1 g) and absolute ethanol (25 mL), saturated with hydrogen, was added 5 mL of the filtrate from a solution of sodium borohydride (500 mg) in ethanol (12 mL) and 2N aqueous sodium hydroxide (0.63 mL). After hydrogen evolution had ceased, the black suspension was treated with 0.7 mL of ethylene diamine.6Alkyne 24 (643 mg, 3.0 mmol) was added and the reaction stirred for 1 hr at 23° C. The reaction was diluted with brine (100 mL), acidified with 5% HCl and extracted with ether (4×50 mL). The ether extract was washed with brine (2×50 mL). Product isolation gave 620 mg of 26 (96% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04560551 |
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| 출처 데이터셋 | uspto-grants-1985_12 |
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| ORD ID | ord-6d96527de97c44c283ca96f9c8228bd4 |
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| 출처 메모 | uspto-grants-1985_12 |
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