HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 15391551, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-(Tert-butyldiphenylsilyloxymethyl)-1,6-dibromohexane | HCID 18790455 | — |
| Reactant | HCID 131719532 | HCID 131719532 | — |
| Product | HCID 15391551 | HCID 15391551 | 75% |
Reaction Steps
Following the same procedure described for the preparation of racemic dibromide, 3-(tert-butyldiphenylsilyloxymethyl)-1,6-dibromohexane, (S)-(-)-3-(tertbutyldiphenylsilyloxymethyl)-1,6-hexanediol (4.85 g, 12.53 mmol) was reacted with N-bromosuccinimide (5.35 g, 30.1 mmol) and triphenylphosphine (7.87 g, 30.1 mmol) CH2Cl2 (150 mL) at 0° C. to afford compound (S)-(-)-3-(tert-butyldiphenylsilyloxymethyl)-1,6-dibromohexane 4.81 (75%) as a clear, colorless oil which was homogenous by TLC (Rf =0.8, 10% EtOAc in hexanes. Both the TLC properties and 1H spectra of this compound were identical in all respects with racemic isomer. MS.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05621098 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-2f23f0b2fd174a2998930669b3ae2887 |
| Source note | uspto-grants-1997_04 |