Bromotrimethylsilane → HCID 57289203, compound

HRID 851434Notes

Reaction equation

HRID 851434 reaction equation
C([O:3][P:4]([CH2:16][C:17]([N:19]1[C@H:27]([C:28]([O:30][CH2:31][O:32][C:33](=[O:38])[C:34]([CH3:37])([CH3:36])[CH3:35])=[O:29])[CH2:26][C:21]2([S:25][CH2:24][CH2:23][S:22]2)[CH2:20]1)=[O:18])([CH2:6][CH2:7][CH2:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:5])C.Br[Si](C)(C)C>ClCCl>[OH:5][P:4]([CH2:16][C:17]([N:19]1[C@H:27]([C:28]([O:30][CH2:31][O:32][C:33](=[O:38])[C:34]([CH3:36])([CH3:35])[CH3:37])=[O:29])[CH2:26][C:21]2([S:22][CH2:23][CH2:24][S:25]2)[CH2:20]1)=[O:18])([CH2:6][CH2:7][CH2:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:3]

Participants

4

Procedure

(S)-7-[[Ethoxy(4-phenylbutyl)phosphinyl]acetyl]-1,4-dithia-7-azaspiro[4.4]nonane-8-carboxylic acid, (2,2-dimethyl-1-oxopropoxy)methyl ester (2.7 g) in dichloromethane (dried over alumina) is treated with bromotrimethylsilane (1.2 ml) via syringe and the reaction mixture is stirred for 16 hours under argon. The solvent and excess bromotrimethylsilane is evaporated in vacuo and the residue is taken up in ethyl acetate and water and stirred for 15 minutes. The layers are separated and the ethyl acetate is washed with 5% potassium sulfate, water, brine dried (MgSO4) and evaporated. The 2.3 g of crude product is chromatographed on silica (75 g) eluting with dichloromethane/methanol/acetic acid (19/0.5/0.5). After stripping solvent 1.9 g of product is left as a glass.

Workup

  1. customThe solvent and excess bromotrimethylsilane is evaporated in vacuo
  2. stirringwater and stirred for 15 minutes
  3. customThe layers are separated
  4. washthe ethyl acetate is washed with 5% potassium sulfate, water, brine
  5. dry with materialdried (MgSO4)
  6. customevaporated
  7. customThe 2.3 g of crude product is chromatographed on silica (75 g)
  8. washeluting with dichloromethane/methanol/acetic acid (19/0.5/0.5)
  9. waitis left as a glass

Sources & evidence

ORD record
ord-7d1af897ecc049df8f2af6fd08e0a0ed
Source dataset
uspto-grants-1983_05
Patent number
US04384123

Reaction notes

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