Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzenepropanol | HCID 31234 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 65935-40-2 | HCID 21418689 | 85% |
Reaction Steps
In a four necked round bottom flask, triphosgene (5.45 g, 55.1 mmol) was dissolved in toluene (80 mL) under argon. After cooling at 0° C., pyridine (4.8 mL, 58.8 mmol) was added dropwise during 1 h and the resulting suspension stirred for further 1 h at 0° C. 3-phenyl-1-propanol (5 mL, 36.8 mmol) was added dropwise in 30 min. After stirring at rt for 24 h, the solid was filtered off and the solvent removed under vacuum, yielding the title compound (6.2 g, 85%) as pale yellow oil, which was used in the next step without further purification. FTIR (cm−1): 3086, 3065, 3027, 2995, 2932, 2862, 1776, 1743, 1603, 1496, 1454, 1262, 1148, 745, 699.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09353075B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-831f1103789645beb64d32149917cc55 |
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| Source note | uspto-grants-2016_05 |
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