Methanol → HCID 178501209, compound
Reaction equation
S(Cl)([Cl:4])(=O)=O.[NH2:6][C@@H:7]1[CH2:12][CH2:11][C@H:10]([C:13]([OH:15])=[O:14])[CH2:9][CH2:8]1.[CH3:16]O>>[ClH:4].[NH2:6][C@@H:7]1[CH2:12][CH2:11][C@H:10]([C:13]([O:15][CH3:16])=[O:14])[CH2:9][CH2:8]1Participants
4
Conditions
- Temperature
- -10 °C
Procedure
5 cm3 of sulfonyl chloride are added dropwise to 50 cm3 of methanol cooled to −10° C. After stirring for 10 minutes at 20° C., 5.0 g of cis-4-aminocyclohexane-1-carboxylic acid are slowly added in fractions. After stirring for 2 hours at ,20° C., the reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa) at 20° C., to give 7.5 g of methyl cis-4-aminocyclohexane-1-carboxylate hydrochloride, in the form of a white powder.
Workup
- stirringAfter stirring for 2 hours at ,20° C.
- concentrationthe reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa) at 20° C.
Sources & evidence
- ORD record
- ord-ee5a4129c26c418eb312d65c6109a6c0
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07166594B2
Reaction notes
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