HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081156Generated: November 2, 2026
Thiophosgene → (3-Isothiocyanatophenyl)boronic acid
https://huagongshe.com/reaction/2081156
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | 3-Aminophenylboronic acid | HCID 92269 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | (3-Isothiocyanatophenyl)boronic acid | HCID 22556042 | — |
Reaction Steps
To a cooled (0° C.) solution of 3-aminophenylboronic acid (2.24 g, 0.013 mol) in acetone (5 ml) was added dropwise a solution of thiophosgene (1 ml, 0.013 mol) in chloroform (5 ml) over a period of 0.5 hour. The reaction mixture was stirred at 0° C. for 1 hour and at room temperature for 12 hours. The solvent was evaporated on a rotary evaporator and the residue was triturated with ether and filtered to remove the triethylamine hydrochloride. The ether solution was evaporated to a brown oil. This was chromatographed on silica gel (30 g) using acetone-chloroform (7:3) as eluent. Fractions containing the product were collected and evaporated to give a light brown solid. This solid was crystallized from ethyl acetate/hexane. M.P. 166°-67° C. Anal. Calcd. for C7H6NSBO2O: C, 46,00; H,3.59; N, 7.67; S, 17.54. Found: C, 46.17; H, 3.48; N, 7.59; S, 17.71.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05183653 |
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| Source dataset | uspto-grants-1993_02 |
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| ORD ID | ord-73d56fd6c6c649b0b3838bf6c0d7e9a6 |
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| Source note | uspto-grants-1993_02 |
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