HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → (3R)-8-(4-isopropylphenoxy)-1-thia-4-azaspiro[4.5]decane-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | L-Cysteine hydrochloride monohydrate | HCID 23462 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 4-(4-Isopropylphenoxy)-1-cyclohexanone | HCID 22467144 | — |
| Solvent | Water | HCID 962 | — |
| Product | (3R)-8-(4-isopropylphenoxy)-1-thia-4-azaspiro[4.5]decane-3-carboxylic acid | HCID 70156069 | 54.7% |
Reaction Steps
In a solvent mixture consisting of 21 ml of ethanol and 9 ml of water were dissolved 3.10 g of 4-(4-isopropylphenoxy)-1-cyclohexanone, 2.35 g of L-cysteine hydrochloride monohydrate and 1.10 g of sodium acetate. The mixture was stirred at ambient temperature for 6 hours. The reaction mixture was concentrated under reduced pressure, and water and ethyl ether were added to the concentrate. The deposited crystal was collected by filtration, and there was obtained 2.45 g of (3R)-8-(4-isopropylphenoxy)-1-thia-4-azaspiro[4.5]decan-3-carboxylic acid as a colorless crystalline product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06384065B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-7a3e02c9157c49828c2b4131da2f3189 |
| Source note | uspto-grants-2002_05 |