HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588697Generated: October 27, 2026
Hydrogen Bromide → 3-(1H-pyrazol-1-ylmethyl)tricyclo[3.3.1.13,7]decane-1-thiol
https://huagongshe.com/reaction/588697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 3-bromotricyclo[3.3.1.13,7]dec-1-ylmethyl-1H-pyrazole | HCID 86681261 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-(1H-pyrazol-1-ylmethyl)tricyclo[3.3.1.13,7]decane-1-thiol | HCID 89498949 | — |
Reaction Steps
A solution of EXAMPLE 26A (2.0 g) and thiourea (2.0 g) in a solvent mixture of acetic acid (20 mL) and 48% aqueous HBr solution (10 mL) was heated to 100° C. for 24 hours. The reaction was concentrated to dryness, and the residue was dissolved in 20% v/v ethanol in water (100 mL). Solid sodium hydroxide (10 g) was added, and the mixture was stirred overnight. The solution was acidified to pH 1 with concentrated HCl solution, and diluted with ethyl acetate (100 mL). The layers were separated, and the aqueous layer was extracted with additional ethyl acetate (2×100 mL). The combined organic layers were washed with water, dried over Na2SO4, filtered, and concentrated. The residue was purified by silica gel chromatography, eluting with a gradient of 10-50% ethyl acetate in hexane, to give the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09227963B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-61ab77765b924dacbaa1ce6e2e567c96 |
|---|
| Source note | uspto-grants-2016_01 |
|---|