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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814163Generated: November 5, 2026

Dichloromethane → HCID 11984183, compound

https://huagongshe.com/reaction/1814163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTin atomHCID 5352426—
ReactantHCID 23112079HCID 23112079—
SolventMethanolHCID 887—
Solvent1,4-Dioxane hydrochlorideHCID 20443148—
ProductHCID 11984183HCID 1198418386%

Reaction Steps

The above product 36B (1.0 g, 3.64 mmol) was refluxed with tin powder (2.2 g, 18.8 mmol) in MeOH (10 mL) and 4M HCl/dioxane (10 mL). After 3 h, the reaction mixture was poured into ice with CH2Cl2 (100 mL). The phases were separated and the aqueous layer was extracted with CH2Cl2 (2×50 mL). The combined organic layers were dried with magnesium sulfate, filtered and evaporated to give the thiol compound 36C as a yellow oil (650 mg, 86%). MS: 207 (M−1)+. Step 4. Preparation of (4′-Trifluoromethyl-biphenyl-4-yl)-methanol (Compound 36D)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875780B2
Source datasetuspto-grants-2005_04
ORD IDord-74b5c1f4e3434ba2a6eb704f6565de3d
Source noteuspto-grants-2005_04