Hydrochloric Acid → (2S)-2-Amino-1-(3-fluorophenyl)-4-methyl-pentane-1-ol hydrochloride

HRID 13127Notes

Reaction equation

HRID 13127 reaction equation
C(OC(=O)[NH:7][C@H:8]([CH:13]([C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([F:21])[CH:16]=1)[OH:14])[CH2:9][CH:10]([CH3:12])[CH3:11])(C)(C)C.[ClH:23]>O1CCOCC1>[ClH:23].[NH2:7][C@@H:8]([CH2:9][CH:10]([CH3:12])[CH3:11])[CH:13]([C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([F:21])[CH:16]=1)[OH:14]

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 86623010HCID 86623010, compound

Product 1

HCID 66812770(2S)-2-Amino-1-(3-fluorophenyl)-4-methyl-pentane-1-ol hydrochloride

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent2×

Procedure

The aforementioned described {(S)-1-[(3-fluorophenyl)-hydroxymethyl]-3-methylbutyl}-carbamic acid tert.-butylester (4.7 g, 15.1 mmol) is dissolved in dioxane (37 mL). After addition of HCl in dioxane (37.7 mL of a 4M solution) the reaction mixture is stirred for 4 h. After evaporation of the solvent the crude product (3.7 g, 99.5%) is used in the next step without further purification.

Workup

  1. customAfter evaporation of the solvent the crude product (3.7 g, 99.5%)
  2. customis used in the next step without further purification

Sources & evidence

ORD record
ord-02040c98ae3a4c6690c4b3023b1340ac
Source dataset
uspto-grants-2010_06
Patent number
US07728030B2

Reaction notes

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