HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583223Generated: October 27, 2026
Carbon tetrabromide → HCID 178444389, compound
https://huagongshe.com/reaction/1583223
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 178444539 | HCID 178444539 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178444389 | HCID 178444389 | 97% |
Reaction Steps
A solution of 3.69 g of (trans-4-pentylcyclohexyl)methanol and 5.51 g of triphenylphosphine in 70 ml of methylene chloride at -30° C. was placed under argon gasification and treated portionwise within 15 minutes with 7.30 g of solid tetrabromomethane so that the internal temperature did not exceed -20° C. After completion of the addition, the cooling bath was removed and the mixture was stirred for a further 18 hours with gradual warming to room temperature. The mixture was then concentrated on a rotary evaporator and the semi-crystalline residue obtained was triturated with 200 ml of warm hexane, filtered and the concentrated filtrate was chromatographed with hexane on a column of silica gel. There were obtained 4.79 g (97%) of trans-1-(bromomethyl)-4-pentylcyclohexane as a colourless liquid which was purified further by distillation; b.p. 82° C./0.08 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04550981 |
|---|
| Source dataset | uspto-grants-1985_11 |
|---|
| ORD ID | ord-d86069d79202459cacb3858ed9f23ceb |
|---|
| Source note | uspto-grants-1985_11 |
|---|