HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylamine → HCID 22117430, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylamine | HCID 7582 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-[(3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)sulfanyl]benzoic acid | HCID 3025918 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22117430 | HCID 22117430 | — |
Reaction Steps
A solution of 1.4 g (4 mmol) of 4-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthylthio)benzoic acid in 100 ml of anhydrous dichloromethane was introduced into a round-bottomed flask, 900 μl (4.4 mmol) of dicyclohexylamine were added and the mixture was stirred for one hour. Next, 320 μl (4.4 mmol) of thionyl chloride were added and the mixture was stirred for one hour. The reaction medium was evaporated to dryness, taken up in anhydrous ethyl ether, the dicyclohexylamine salt filtered off and the filtrate evaporated. 1.5 g (100%) of the crude acid chloride was recovered which was used as such in the continuation of the synthesis to follow.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06015569 |
| Source dataset | uspto-grants-2000_01 |
| ORD ID | ord-9eb5a1fb96a2480f94162004cbd7e371 |
| Source note | uspto-grants-2000_01 |