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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337270Generated: October 29, 2026

Triethylamine → 3-(2,6-Dimethylbenzyloxy)-2-methoxybenzyl methanesulfonate

https://huagongshe.com/reaction/337270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 66959407HCID 66959407—
SolventDichloromethaneHCID 6344—
Product3-(2,6-Dimethylbenzyloxy)-2-methoxybenzyl methanesulfonateHCID 86657009—

Reaction Steps

To a solution of (3-(2,6-dimethylbenzyloxy)-2-methoxyphenyl)methanol (Step B, 9.5 g, 32.7 mmol) and triethylamine (5.80 g, 57.4 mmol) in dry CH2Cl2 (100 ml) was added drop wise methanesulfonyl chloride (3.5 ml, 45 mmol) at 0° C. under argon. The reaction mixture was warmed to room temperature for 6 hours or until all the starting material is consumed, neutralized with cooled 10% Na2CO3 and extracted with CH2Cl2. The organic layer was concentrated, and purified by flash chromatography on a silica gel column (hex: methylene chloride 2:1) to give the title compound as light yellow oil

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889724B2
Source datasetuspto-grants-2014_11
ORD IDord-5efbc75b3aa648ffbfa85a2cc98cc9a5
Source noteuspto-grants-2014_11