HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 11241959, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | HCID 11253594 | HCID 11253594 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11241959 | HCID 11241959 | — |
Reaction Steps
A solution of 4-acetoxy-2-chloro-5-methoxybenzoic acid (8.6 g, 35.2 mmol) and triethylamine (8.9 g, 88 mmol) in dry dichloromethane (100 ml) was cooled to 0° C. and ethylchloroformate (7.6 g, 70 mmol) was added at such a rate that the temperature stayed below 5° C. After 1 h cyclopropylamine (6.0 g, 105 mmol) was added. After stirring overnight at room temperature the organic phase was washed with water (2×200 ml). Drying over magnesium sulfate was followed by reduction of the solvent volume to half. Petrol ether was added and the product was filtered off. Yield 570 mg, 6.7%, mp 214-216° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06207662B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-ab2853d628fa49c28b0b7a60f7e5f398 |
| Source note | uspto-grants-2001_03 |