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Hydrochloric Acid → HCID 9942683, compound

HRID 1612686
Notes
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Reaction equation

HRID 1612686 reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][P:5]([CH:8](OCC)OCC)(=[O:7])[OH:6].[CH2:15]([SH:18])[CH2:16][SH:17].Cl>C(O)(=O)C>[NH2:1][CH2:2][CH2:3][CH2:4][P:5]([CH:8]1[S:18][CH2:15][CH2:16][S:17]1)(=[O:7])[OH:6]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 109021,2-EthanedithiolHCID 107699Cgp 35348

Product 1

HCID 9942683HCID 9942683, compound

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Procedure

To a solution of 0.90 g (4.0 mmol) of 3-aminopropyl(diethoxymethyl)phosphinic acid in 10 ml of glacial acetic acid at 0° there are added 0.38 ml (4,4 mmol) of ethane-1,2-dithiol, followed by addition of 2 ml of concentrated hydrochloric acid over a period of 5 min. The mixture is allowed to warm to room temperature and is then stirred for 18 hours. After removal of acetic and hydrochloric acids under high vacuum, the residue is chromatographed (Opti-Up® C12 50%, water) and recrystallized from methanol to yield 3-aminopropyl(1,3-dithiolan-2-yl)phosphinic acid, m.p. 272°-274°.

Workup

  1. customAfter removal of acetic and hydrochloric acids under high vacuum
  2. customthe residue is chromatographed (Opti-Up® C12 50%, water)
  3. customrecrystallized from methanol

Sources & evidence

ORD record
ord-49637b039b6d4ec8a25a64a8a3ae8794
Source dataset
uspto-grants-1993_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05190933

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes