Hydrochloric Acid → HCID 178479213, compound
Reaction equation
C(OC(=O)[NH:7][CH2:8][CH2:9][C@H:10]1[CH2:13][C@@H:12]([CH:14]([OH:23])[CH2:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH2:11]1)(C)(C)C.[ClH:25]>O1CCOCC1>[ClH:25].[NH2:7][CH2:8][CH2:9][C@@H:10]1[CH2:11][C@H:12]([CH:14]([OH:23])[CH2:15][CH2:16][C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH2:13]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 0.8 g of cis-{2-[3-(1-hydroxy-3-phenyl-propyl)-cyclobutyl]-ethyl}-carbamic acid tert-butyl ester and 25 mL of 4N HCl in dioxane was stirred at room temperature for 2 h, then concentrated to dryness and triturated with 50 mL of 5% ether in hexane and the solvents decanted. Drying under vacuum gave 0.8 g of the product as an amber resin: LCMS (m+1)=234.6.
Workup
- concentrationconcentrated to dryness
- customtriturated with 50 mL of 5% ether in hexane
- customthe solvents decanted
- customDrying under vacuum
Sources & evidence
- ORD record
- ord-622a010b73bc4c32b75043e4d5a577a3
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07452893B2
Reaction notes
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