HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375201Generated: October 28, 2026
Chlorodifluoromethane → HCID 18930396, compound
https://huagongshe.com/reaction/375201
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorodifluoromethane | HCID 6372 | — |
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18930395 | HCID 18930395 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 18930396 | HCID 18930396 | — |
Reaction Steps
A solution of ethyl 5-(p-chlorophenyl)-4-thiocyanatopyrrole-2-carboxylate (76.7 mg, 0.25 mmol) in 2-propanol is treated with sodium borohydride (11.0 mg, 0.29 mmol) under nitrogen, heated to 70° C. for ten minutes, cooled to room temperature, treated with a solution of potassium hydroxide (16.8 mg, 0.30 mmol) in 2-propanol, treated with tributylphosphine (81.2 mg, 0.4 mmol), heated to 65°-70° C. and treated with excess chlorodifluoromethane for one hour. Additional tributylphosphine (81.2 mg, 0.4 mmol) is added to the reaction mixture and the addition of chlorodifluoromethane is continued for 30 minutes. The mixture is then poured into brine and extracted with ethyl acetate. The combined organic extracts are washed with water, dried over anhydrous soidum sulfate and concentrated in vacuo to obtain a liquid. Flash chromatography of the liquid using silica gel and a 1:10 ethyl acetate/hexanes solution gives the title product as a white solid (42.6 mg, mp 113°-117° C.) which is identified by 1HNMR and 13CNMR spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05484807 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-ff2fd5d8ee4d44a2bf9d3084ebcaa497 |
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| Source note | uspto-grants-1996_01 |
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